Journal Articles

450.  “On the Pelletier and Caventou (1817, 1818) Papers on Chlorophyll and Beyond,” Govindjee, G.; Stirbet, A.; Lindsey, J. S.; Scheer, H. Photosynth. Res. 2024, 160, 55–60. DOI: 10.1007/s11120-024-01081-x

449.  “Light-Scattering in Absorption Spectra: A Literature Survey of Examples and Corrections,” Taniguchi, M.; Lindsey, J. S.; Proc. SPIE 2024, 12862, 128620B. DOI: 10.1117/12.3000407

447.  “Chlorin–Dextran Conjugates for Brightness Enhancement in Water,” Liu, S.; Lindsey, J. S.; Taniguchi, M. Proc. SPIE 2024, 12862, 128620A. DOI: 10.1117/12.3000409

446.  “Rapid Screening of Dyes for Self-Aggregation, Adsorption, and Metabolic Integrity – Quantitative Metrics as a Prelude to Biological Studies,” Liu, Q.; Taniguchi, M.; Goel, S.; Lindsey, J. S. Dyes Pigments 2024, 223, 111914. DOI: 10.1016/j.dyepig.2023.111914

445.     “Synthesis of Chiral Hexynones for Use as Precursors to Native Photosynthetic Hydroporphyrins,” Chau Nguyen, K.; Chung, D. T. M.; Nalaoh, P.; Lindsey, J. S. New J. Chem. 2024, 48, 2097–2117. DOI: 10.1039/D3NJ03900E

444.  “Tolyporphins – Exotic Tetrapyrrole Pigments in a Cyanobacterium – A Review,” Nguyen, K.-U.; Zhang, Y.; Liu, Q.; Zhang, R.; Jin, X.; Taniguchi, M.; Miller, E. S.; Lindsey, J. S. Molecules 2023, 28, 6132. DOI: 10.3390/molecules28166132 

443.  “Investigation of Amylose and Tailored Amylose Matrices for Scavenging Iodide” Dou, J.; Sato, D.; Son, J.; Liu, Q.; Lindsey, J. S. Proc. SPIE 2023, 12663, 1266305. DOI: 10.1117/12.2676276

442.  “Synthesis of a BC-Dihydrodipyrrin Building Block of Bacteriochlorophyll a,” Chau Nguyen, K.; Lindsey, J. S. J. Org. Chem. 2023, 88, 11205–11216. DOI: 10.1021/acs.joc.3c01216

  441. "Synthesis of model Southern rim structures of photosynthetic tetrapyrroles and phyllobilins," Nguyen Tran, A. T.; Wu, Z.; Chung, D. T. M.; Nalaoh, P.; Lindsey, J. S. New J. Chem. 2023, 47, 13626–13637. DOI: 10.1039/D3NJ02515B

440.  “Bacteriochlorin Syntheses – Status, Problems, and Exploration,” Tran, V.-P.; Wang, P.; Matsumoto, N.; Liu, S.; Jing, H.; Nalaoh, P.; Chau Nguyen, K.; Taniguchi, M.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2023, 27, 1502–1551. DOI: 10.1142/S1088424623501171

439.  “Tethered Indoxyl-Glucuronides for Enzymatically Triggered Cross-linking” Son, J.; Wu, Z.; Dou, J.; Fujita, H.; Cao, P.-L. D.; Liu, Q.; Lindsey, J. S. Molecules 2023, 28, 4143. DOI: 10.3390/molecules28104143

438. “Digitization of Print-based Absorption and Fluorescence Spectra – Extracting Clarity from Clutter,” Taniguchi, M.; Wu, Z.; Sterling, C. D.; Lindsey, J. S. Proc. SPIE 2023, 12398, 1239806. DOI: 10.1117/12.2651694

437.  “Four Routes to 3-(3-Methoxy-1,3-dioxopropyl)pyrrole, a Core Motif of Rings C and E in Photosynthetic Tetrapyrroles,” Chau Nguyen, K.; Nguyen Tran, A. T.; Wang, P.; Zhang, S.; Wu, Z.; Taniguchi, M.; Lindsey, J. S. Molecules 2023, 28, 1323. DOI: 10.3390/molecules28031323

436.  “Indoxyl-Glucosides Bearing Tethers for Enzymatically Triggered Cross-linking,” Sato, D.; Wu, Z.; Dou, J.; Son, J.; Lindsey, J. S. New J. Chem. 2023, 47, 8223–8242. DOI: 10.1039/d2nj06267d

435. "Absorption and Fluorescence Spectra of Open-chain Tetrapyrrole Pigments – Bilirubins, Biliverdins, Phycobilins, and Synthetic Analogues,” Taniguchi, M.; Lindsey, J. S. J. Photochem. Photobiol. C: Photochem. Rev. 2023, 55, 100585. DOI: 10.1016/j.jphotochemrev.2023.100585

434. “Porphyrin building blocks bearing two or four divergent ethynes,” Cao, P.-L. D.; Wu, Z.; Rong, J.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2023, 27, 1049–1058. DOI: 10.1142/S1088424623500219

433. “Investigation of a Bacteriochlorin-containing Pentad for Panchromatic Light-Harvesting and Charge Separation,” Jing, H.; Magdaong, N. C. M.; Diers, J. R.; Kirmaier, C.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Phys. Chem. Chem. Phys. 2023, 25, 1781–1798. DOI: 10.1039/D2CP05400K 

432. “Tailoring the AIE Chromogen 2-(2-Hydroxyphenyl)benzothiazole for Use in Enzyme-Triggered Molecular Brachytherapy,” Wu, Z.; Dou, J.; Nguyen, K.-U.; Eppley, J. C.; Siwawannapong, K.; Zhang, Y.; Lindsey, J. S. Molecules 2022, 27, 8682. DOI: 10.3390/molecules27248682

431.  “Dyads with Tunable Near-Infrared Donor–Acceptor Excited-State Energy Gaps: Molecular Design and Förster Analysis for Ultrafast Energy Transfer,” Jing, H.; Magdaong, N. C. M.; Diers, J. R.; Kirmaier, C.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Phys. Chem. Chem. Phys. 2023, 25, 1827–1847. DOI: 10.1039/d2cp04689j 

430.  “Panchromatic Absorbers Tethered for Bioconjugation or Surface Attachment,” Liu, R.; Rong, J.; Wu, Z.; Taniguchi, M.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Molecules 2022, 27, 6501. DOI: 10.3390/molecules27196501

429.  “Balancing Panchromatic Absorption and Multistep Charge Separation in a Compact Molecular Architecture,” Roy, A.; Magdaong, N. C. M.; Jing, H.; Rong, J.; Diers, J. R.; Kang, H. S.; Niedzwiedzki, D. M.; Taniguchi, M.; Kirmaier, C.; Lindsey, J. S.; Bocian, D. F.; Holten, D. Phys. Chem. A 2022, 50, 9353–9365. DOI: 10.1021/acs.jpca.2c06040

428. “Digital Database of Absorption Spectra of Diverse Flavonoids Enables Structural Comparisons and Quantitative Evaluations,” Taniguchi, M.; LaRocca, C.; Bernat, J. D.; Lindsey, J. S. J. Nat. Prod. 2023,  86, 1087–1119. DOI: 10.1021/acs.jnatprod.2c00720

427. “Probing the Effects of Electronic–Vibrational Resonance on the Rate of Excited-State Energy Transfer in Bacteriochlorin Dyads,” Magdaong, N. C. M.; Jing, H.; Diers, J. R.; Kirmaier, C.; Lindsey, J. S.; Bocian, D. F.; Holten, D. J. Phys. Chem. Lett. 2022, 13, 7906–7910. DOI: 10.1021/acs.jpclett.2c02154

426. “Phyllobilins – Bioactive Natural Products Derived from Chlorophyll ­– Plant Origins, Structures, Absorption Spectra, and Biomedical Properties,” Karg, C. A.; Taniguchi, M.; Lindsey, J. S.; Moser, S. Planta Medica 2023, 89, 637–662.DOI: 10.1055/a-1955-4624

425. “Dihydrooxazine Byproduct of a McMurry–Melton Reaction En Route to a Synthetic Bacteriochlorin,” Tran, V.-P.; Matsumoto, N.; Nalaoh, P.; Jing, H.; Chen, C.-Y.; Lindsey, J. S. Organics 2022, 3, 262–274. DOI: 10.3390/org3030019

424. “Simple Dipyrrin Analogues of Prodigiosin for Use as Colistin Adjuvants,” Siwawannapong, K.; Nemeth, A. M.; Melander, R. J.; Rong, J.; Davis, J. R.; Taniguchi, M.; Carpenter, M. E.; Lindsey, J. S.; Melander, C. ChemMedChem 2022, e202200286. DOI: 10.1002/cmdc.202200286

423. “Synthesis and Properties of Metalated Tetradehydrocorrins,” Sun, R.; Liu, M.; Wang, P.; Qin, Y.; Schnedermann, C.; Maher, A. G.; Zheng, S.-L.; Liu, S.; Chen, B.; Zhang, S.; Dogutan, D. K.; Lindsey, J. S.; Nocera, D. G. Inorg. Chem. 2022, 61, 12308–12317. DOI: 10.1021/acs.inorgchem.2c01642

422. “Chasing the green echiuran worm Bonellia in tidal pools of Okinawa,” Taniguchi, M.; Taniguchi, M.; Zhang, R.; Goto, R.; Lindsey, J. S. Proc. SPIE 2022, 11979, 119790A. DOI: 10.1117/12.2608722

421. “De Novo Synthesis of Bacteriochlorins Bearing Four Trideuteriomethyl Groups,” Jing, H.; Tang, Q.; Bocian, D. F.; Lindsey, J. S. Organics 2022, 3, 22–37. DOI: 10.3390/org3010002

420.  “Meso bromination and derivatization of synthetic bacteriochlorins,” Jing, H.; Liu, S.; Jiang, J.; Tran, V.-P.; Rong, J.; Wang, P.; Lindsey, J. S. New J. Chem. 2022, 46, 5556–5572. DOI: 10.1039/D1NJ05853C

419. “Synthesis of bacteriochlorins bearing diverse β-substituents,” Jing, H.; Wang, P.; Chen, B.; Jiang, J.; Vairaprakash, P.; Liu, S.; Rong, J.; Chen, C.-Y.; Nalaoh, P.; Lindsey, J. S. New J. Chem. 2022, 46, 5534–5555. DOI: 10.1039/D1NJ05852E

418. “Beyond Green with Synthetic Chlorophylls – Connecting Structural Features with Spectral Properties,” Taniguchi, M.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Photochem. Photobiol. C 2022, 100513. DOI: 10.1016/j.jphotochemrev.2022.100513

417. “Phenylene-linked tetrapyrrole arrays containing free base and diverse metal chelate forms – Versatile synthetic architectures for catalysis and artificial photosynthesis,” Jing, H.; Rong, J.; Taniguchi, M.; Lindsey, J. S. Coord. Chem. Rev. 2022, 456, 214278. DOI: 10.1016/j.ccr.2021.214278

416. “Electronic Structure and Excited-State Dynamics of Rylene–Tetrapyrrole Panchromatic Absorbers,” Rong, J.; Magdaong, N. C. M.; Taniguchi, M.; Diers, J. R.; Niedzwiedzki, D. M.; Kirmaier, C.; Lindsey, J. S.; Bocian, D. F.; Holten, D. J. Phys. Chem. A 2021, 125, 7900–7919. DOI: 10.1021/acs.jpca.1c05771

415.  “Identification of Putative Biosynthetic Gene Clusters for Tolyporphins in Multiple Filamentous Cyanobacteria,” Jin, X.; Zhang, Y.; Zhang, R.; Nguyen, K.-U.; Lindsey, J. S.; Miller, E. S. Life 2021, 11, 758. DOI: 10.3390/life11080758

414.  “Synthesis of AD-Dihydrodipyrrins Equipped with Latent Substituents of Native Chlorophylls and Bacteriochlorophylls,” Wang, P.; Lindsey, J. S. J. Org. Chem. 2021, 86, 11794–11811. DOI: 10.1021/acs.joc.1c01239

413.  “Synthesis of model bacteriochlorophylls containing substituents of native rings A, C and E,” Chung, D. T. M.; Tran, P. V.; Chau Nguyen, K.; Wang, P.; Lindsey, J. S. New J. Chem. 2021, 45, 13302–13316. DOI: 10.1039/D1NJ02469H

412.  “Design, Synthesis, and Utility of Defined Molecular Scaffolds,” Sato, D.; Wu, Z.; Fujita, H.; Lindsey, J. S. Organics 2021, 2, 161–273. DOI: 10.3390/org2030013

411.  “Fluorescence Assay for Tolyporphins Amidst Abundant Chlorophyll in Crude Cyanobacterial Extracts,” Nguyen, K.-U.; Zhang, R.; Taniguchi, M.; Lindsey, J. S. Photochem. Photobiol. 2021, 97, 1507–1515. DOI: 10.1111/php.13474

410.  “A perspective on the redox properties of tetrapyrrole macrocycles,” Diers, J. R.; Kirmaier, C.; Taniguchi, M.; Lindsey, J. S.; Bocian, D. F.; Holten, D. Phys. Chem. Chem. Phys. 2021, 23, 19130–19140. DOI: 10.1039/D1CP01943K

409.  "Tolyporphins A–R, unusual tetrapyrrole macrocycles in a cyanobacterium from Micronesia, assessed quantitatively from the culture HT-58-2," O’Donnell, T. J.; Gurr, J. R.; Dai, J.; Taniguchi, M.; Williams, P. G.; Lindsey, J. S. New J. Chem. 2021, 45, 11481–11494. DOI: 10.1039/D1NJ02108G

408.  "Considerations of the biosynthesis and molecular diversity of tolyporphins," Lindsey, J. S. New J. Chem. 2021, 45, 12097–12107. DOI: 10.1039/d1nj01761f

407.  "Natural Product Gene Clusters in the Filamentous Nostocales Cyanobacterium HT-58-2," Jin, X.; Miller, E. S.; Lindsey, J. S. Life 2021, 11, 356. DOI: 10.3390/life11040356

406.  "In-Situ, Protein-Mediated Generation of a Photochemically Active Chlorophyll Analog in a Mutant Bacterial Photosynthetic Reaction Center," Magdaong, N. C. M.; Buhrmaster, J. C.; Faries, K. M.; Liu, H.; Tira, G. A.; Lindsey, J. S.; Hanson, D. K.; Holten, D.; Laible, P. D.; Kirmaier, C. Biochemistry 2021, 60, 1260–1275. DOI: 10.1021/acs.biochem.1c00137

405.  "PhotochemCAD Spectra Viewer for Web-based Visualization of Absorption and Fluorescence Spectra," Wu, Z.; Kittinger, A.; Norcross, A. E.; Taniguchi, M.; Lindsey, J. S. Proc. SPIE 2021, 11660, 116600I. DOI: 10.1117/12.2577840

404.  "The fluorescence quantum yield parameter in Förster resonance energy transfer (FRET) – Meaning, misperception, and molecular design," Lindsey, J. S.; Taniguchi, M.; Bocian, D. F.; Holten, D. Chem. Phys. Rev. 2021, 2, 011302. DOI: 10.1063/5.0041132

403.  "Single-Fluorophore Single-Chain Nanoparticle Undergoes Fluorophore-Driven Assembly with Fluorescence Features Retained in Physiological Milieu," Liu, S.; Liu, R.; Lindsey, J. S. ACS Appl. Polym. Mater. 2021, 3, 1767–1776. DOI: 10.1021/acsapm.0c01313

402.  "Comprehensive review of photophysical parameters (ε, Φf, τS) of tetraphenylporphyrin (H2TPP) and zinc tetraphenylporphyrin (ZnTPP) – Critical benchmark molecules in photochemistry and photosynthesis," Taniguchi, M.; Lindsey, J. S.; Bocian, D. F.; Holten, D. J. Photochem. Photobiol. C: Photochem. Rev. 2021, 46, 100401. DOI: 10.1016/j.jphotochemrev.2020.100401

401.  "Study of conditions for streamlined assembly of a model bacteriochlorophyll from two dihydrodipyrrin halves," Chau Nguyen, K.; Wang, P.; Lindsey, J. S. New J. Chem. 2021, 45, 569–581. DOI: 10.1039/D0NJ04855K

400.  "Aqueous solubilization of hydrophobic tetrapyrrole macrocycles by attachment to an amphiphilic single-chain nanoparticle (SCNP)," Liu, R.; Liu, S.; Hu, G.; Lindsey, J. S. New J. Chem. 2020, 44, 21293–21308. DOI: 10.1039/D0NJ04413J

399.  "Photophysical Properties and Electronic Structure of Zinc(II) Porphyrins Bearing 0–4 meso-Phenyl Substituents: Zinc Porphine to Zinc Tetraphenylporphyrin (ZnTPP)," Magdaong, N. C. M.; Taniguchi, M.; Diers, J. R.; Niedzwiedzki, D. M.; Kirmaier, C.; Lindsey, J. S.; Bocian, D. F.; Holten, D. J. Phys. Chem. A 2020, 124, 7776–7794. DOI: 10.1021/acs.jpca.0c06841

398.  "Absorption and Fluorescence Spectral Database of Chlorophylls and Analogues," Taniguchi, M.; Lindsey, J. S. Photochem. Photobiol. 2021, 97, 136–165.  DOI: 10.1111/php.13319

397.  "Engineering of an archaeal phosphodiesterase to trigger aggregation-induced emission (AIE) of synthetic substrates," Zhang, Y.; Wu, Z.; Takashima, I.; Nguyen, K.-U.; Matsumoto, N.; Lindsey, J. S. New J. Chem. 2020, 44, 14266–14277. DOI: 10.1039/D0NJ03208E

396.  "Peptide-based scaffolds for in vivo immobilization and enzyme attachment in therapeutic applications," Lee, D. L.; Chin, H.-L. M.; Knudsen, C. G.; Mayers, G. L.; Rose, D. S.; Skogstrom, R. K.; Palzkill, T.; Fujita, H.; Zhang, Y.; Wu, Z.; Lindsey, J. S. Proc. SPIE 2020, 11477, 1147708. DOI: 10.1117/12.2566895

395.  "Fourfold alkyl wrapping of a Copper(II) Porphyrin Thwarts Macrocycle π–π stacking in a compact supramolecular package," Nalaoh, P.; Bureekaew, S.; Promarak, V.; Lindsey, J. S. Acta Cryst. C  2020, C76, 647–654. DOI: 10.1107/S2053229620007172

394.  "Crystal Structure of 1,9-Dibromo-5-phenyldipyrrin, Tetrapyrrole Synthesis Derivative and Free Base Ligand of BODIPY Building Blocks," O’Shea, D. F.; Sommer, R. D.; Taniguchi, M.; Lindsey, J. S. X-Ray Struct. Anal. Online 2020, 36, 21–22. DOI: 10.2116/xraystruct.36.21

393.  "Riley Oxidation of Heterocyclic Intermediates on Paths to Hydroporphyrins – A Review," Wang, P.; Lindsey, J. S. Molecules 2020, 25, 1858. DOI: 10.3390/molecules25081858

392.  "Asymmetric Synthesis of a Bacteriochlorophyll Model Compound Containing trans-Dialkyl Substituents in Ring D," Chau Nguyen, K.; Wang, P.; Sommer, R. D.; Lindsey, J. S. J. Org. Chem. 2020, 85, 6605–6619. DOI: 10.1021/acs.joc.0c00608

391.  "Green Plants, Red Glow – Looking at Chlorophyll’s Red Fluorescence as an Exercise in Exploring Photosynthesis, Agriculture, and Global Ecology," Nguyen, K.-U.; Ratchford, A. R.; Painter, J. L.; Polmanteer, R.; Norcross, A. E.; Lindsey, J. S. Science Scope 2021, 44(6), 56–63. (July/August issue)

390.  "Analysis of Wikipedia pageviews to identify popular chemicals," Cao, Y.; Mehta, H.; Norcross, A. E.; Taniguchi, M.; Lindsey, J. S. Proc. SPIE 2020, 11256, 112560I. DOI: 10.1117/12.2542835

389.  "Absorption and fluorescence spectra of organic compounds from 40 sources: archives, repositories, databases, and literature search engines," Taniguchi, M.; Lindsey, J. S. Proc. SPIE 2020, 11256, 112560J. DOI: 10.1117/12.2542859

388.  "Chromogenic agents built around a multifunctional double-triazine framework for enzymatically triggered cross-linking under physiological conditions," Fujita, H.; Zhang, Y.; Wu, Z.; Lindsey, J. S. New J. Chem. 2020, 44, 3856–3867. DOI: 10.1039/C9NJ06187H

387.  "Use of the Nascent Isocyclic Ring to Anchor Assembly of the Full Skeleton of Model Chlorophylls,” Wang, P.; Lu, F.; Lindsey, J. S. J. Org. Chem. 2020, 85, 702–715. DOI: 10.1021/acs.joc.9b02770

386.  “Enzymatically triggered chromogenic cross-linking agents under physiological conditions,” Fujita, H.; Dou, J.; Matsumoto, N.; Wu, Z.; Lindsey, J. S. New J. Chem. 2020, 44, 719–743. DOI: 10.1039/C9NJ04126E

385.  “Bacteriochlorin–bis(spermine) conjugate affords efficient photodynamic inactivation of bacteria,” Ballatore, M. B.; Milanesio, M. E.; Fujita, H.; Lindsey, J. S.; Durantini, E. N. J. Biophotonics  2020, 13, e201960061. DOI: 10.1002/jbio.201960061

384.  “Bioconjugatable synthetic chlorins rendered water-soluble with three PEG-12 groups via click chemistry,” Matsumoto, N.; Taniguchi, M.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2020, 24, 362–378. DOI: 10.1142/S1088424619501219

383.  “Synthesis of the Ring C Pyrrole of Native Chlorophylls and Bacteriochlorophylls,” Wang, P.; Nguyen, K. C.; Lindsey, J. S. J. Org. Chem. 2019, 84, 11286–11293. DOI: 10.1021/acs.joc.9b01650

382.  “Self-assembly with fluorescence readout in a free base dipyrrin–polymer triggered by metal ion binding in aqueous solution,” Liu, R.; Vairaprakash, P.; Lindsey, J. S. New J. Chem. 2019, 43, 9711–9724. DOI: 10.1039/C9NJ01787A

 381.  “New molecular design for blue BODIPYs,” Wu, Z.; Fujita, H.; Magdaong, N. C. M.; Diers, J. R.; Hood, D.; Allu, S.; Niedzwiedzki, D. M.; Kirmaier, C.; Bocian, D. F. Holten, D.; Lindsey, J. S. New J. Chem. 2019, 43, 7233–7242. DOI: 10.1039/C9NJ01114E

380.  “Annulated bacteriochlorins for near-infrared photophysical studies,” Fujita, H.; Jing, H.; Krayer, M.; Allu, S.; Veeraraghavaiah, G.; Wu, Z.; Jiang, J.; Diers, J. R.; Magdaong, N. C. M.; Mandal, A. K.; Roy, A.; Niedwiedzki, D. M.; Kirmaier, C.; Bocian, D. F.; Holten, D.; Lindsey, J. S. New J. Chem. 2019, 43, 7209–7232.381. DOI: 10.1039/C9NJ01113G

379.  “Developing a user community in the photosciences: a website for spectral data and access to PhotochemCAD,” Guo, Y.; Xu, Z.; Norcross, A. E.; Taniguchi, M.; Lindsey, J. S. Proc. SPIE 2019, 10893, 108930O. DOI: 10.1117/12.2508077

378.  “Single-Polymer–Single-Cargo Strategy Packages Hydrophobic Fluorophores in Aqueous Solution with Retention of Inherent Brightness,” Liu, R.; Lindsey, J. S. ACS Macro Lett. 2019, 8, 79–83. Erratum: ACS Macro Lett. 2019, 8, 154–154. DOI: 10.1021/acsmacrolett.8b00907

377.  “Heuristics from Modeling of Spectral Overlap in Förster Resonance Energy Transfer (FRET),” Qi, Q.; Taniguchi, M.; Lindsey, J. S. J. Chem. Inf. Model. 2019, 59, 652–667. DOI: 10.1021/acs.jcim.8b00753

376.  “Cellular localization of tolyporphins, unusual tetrapyrroles, in a microbial photosynthetic community determined using hyperspectral confocal fluorescence microscopy,” Barnhart-Dailey, M.; Zhang, Y.; Zhang, R.; Anthony, S. M.; Aaron, J. S.; Miller, E. S.; Lindsey, J. S.; Timlin, J. A. Photosyn. Res. 2019, 141, 259–271. DOI: 10.1007/s11120-019-00625-w

375.  “Unusual Stability of a Bacteriochlorin Electrocatalyst Under Reductive Conditions. A Case Study on CO2 Conversion to CO,” Jiang, J.; Matula, A. J.; Swierk, J. R.; Romano, N.; Wu, Y.; Batista, V.; Crabtree, R. H.; Lindsey, J. S.; Wang, H.; Brudvig, G. W. ACS Catalysis 2018, 8, 10131–10136. DOI: 10.1021/acscatal.8b02991

374.  “Origin of Panchromaticity in Multichromophore–Tetrapyrrole Arrays,” Yuen, J.; Diers, J. R.; Alexy, E. J.; Roy, A.; Mandal, A. K.; Kang, H. S.; Niedzwiedzki, D. M.; Kirmaier, C.; Lindsey, J. S.; Bocian, D. F.; Holten, D. J. Phys. Chem. A 2018, 122, 7181–7201. DOI: 10.1021/acs.jpca.8b06815

373.  “Genome sequence, metabolic properties and cyanobacterial attachment of Porphyrobacter sp. HT-58-2 isolated from a filamentous cyanobacterium–microbial consortium,” Hughes, R.-A.; Jin, X.; Zhang, Y.; Zhang, R.; Tran, S.; Williams, P. G.; Lindsey, J. S.; Miller, E. S. Microbiol. 2018, 164, 1229–1239. DOI: 10.1099/mic.0.000706

372.  “Synthesis of arrays containing porphyrin, chlorin, and perylene-imide constituents for panchromatic light-harvesting and charge separation,” Hu, G.; Kang, H. S.; Mandal, A. K.; Roy, A.; Kirmaier, C.; Bocian, D. F.; Holten, D.; Lindsey, J. S.  RSC Adv. 2018, 8, 23854–23874. DOI: 10.1039/C8RA04052D

371.  “Total synthesis campaigns toward chlorophylls and related natural hydroporphyrins – diverse macrocycles, unrealized opportunities,” Liu, Y.; Zhang, S.; Lindsey, J. S. Nat. Prod. Rep. 2018, 35, 879–901. DOI: 10.1039/C8NP00020D

370.  “Red and near-infrared fluorophores inspired by chlorophylls: consideration of practical brightness in multicolor flow cytometry and biomedical sciences,” Taniguchi, M.; Hu, G.; Liu, R.; Du, H.; Lindsey, J. S. Proc. SPIE 2018, 10508, 1050806. DOI: 10.1117/12.2302709

369.  “Mass spectrometric detection of chlorophyll a and the tetrapyrrole secondary metabolite tolyporphin A in the filamentous cyanobacterium HT-58-2. Approaches to high-throughput screening of cyanobacteria,” Zhang, Y.; Zhang, R.; Nazari, M.; Bagley, M. C.; Miller, E. S.; Williams, P. G.; Muddiman, D. C.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2017, 21, 759–768. DOI: 10.1142/S108842461750078X

368.  “Chlorophyll-Inspired Red-Region Fluorophores: Building Block Syntheses and Studies in Aqueous Media,” Liu, R.; Liu, M.; Hood, D.; Chen, C. -Y.; MacNevin, C. J.; Holten, D.; Lindsey, J. S. Molecules 2018, 23, 130 (30 pages). Special issue: Advanced Functional Dyes. DOI: 10.3390/molecules23010130

367.  “Expanding Covalent Attachment Sites of Nonnative Chromophores to Encompass the C-Terminal Hydrophilic Domain in Biohybrid Light-Harvesting Architectures,” Hood, D.; Sahin, T.; Parkes-Loach, P. S.; Jiao, J.; Harris, M. A.; Dilbeck, P.; Niedzwiedzki, D. M.; Kirmaier, C.; Loach, P. A.; Bocian, D. F.; Lindsey, J. S.; Holten, D. ChemPhotoChem 2018, 2, 300–303. DOI: 10.1002/cptc.201700182

366.  “Tailoring Panchromatic Absorption and Excited-State Dynamics of Tetrapyrrole–Chromophore (Bodipy, Rylene) Arrays – The Interplay of Orbital Mixing and Configuration Interaction,” Mandal, A. K.; Diers, J. R.; Niedzwiedzki, D. M.; Hu, G.; Liu, R.; Alexy, E. J.; Lindsey, J. S.; Bocian, D. F.; Holten, D. J. Am. Chem. Soc. 2017, 139, 17547–17564. DOI: 10.1021/jacs.7b09548

365.  “Quantitation of Tolyporphins, Diverse Tetrapyrrole Secondary Metabolites with Chlorophyll-like Absorption, From a Filamentous Cyanobacterium–Microbial Community,” Zhang, Y.; Zhang, R.; Hughes, R.-A.; Dai, J.; Gurr, J. R.; Williams, P. G.; Miller, E. S.; Lindsey, J. S. Phytochem. Anal. 2017, 205–216. DOI: 10.1002/pca.2735

364.  “Database of Absorption and Fluorescence Spectra of >300 Common Compounds for use in PhotochemCAD,” Taniguchi, M.; Lindsey, J. S. Photochem. Photobiol. 2018, 290–327. DOI: 10.1111/php.12860

363.  “PhotochemCAD 3: Diverse Modules for Photophysical Calculations with Access to Multiple Spectral Databases,” Taniguchi, M.; Du, H.; Lindsey, J. S. Photochem. Photobiol. 2018, 277–289. DOI: 10.1111/php.12862

362.  “Characterization of Hydroporphyrins Covalently Attached to Si(100),” Jiao, J.; Miao, Y.; Holten, D.; Lindsey, J. S.; Bocian, D. F. J. Porphyrins Phthalocyanines 2017, 21, 453–464. DOI: 10.1142/S1088424617500547

361.  “Synthesis of tailored hydrodipyrrins and examination in directed routes to bacteriochlorins and tetradehydrocorrins,” Zhang, S.; Reddy, M. N.; Mass, O.; Kim, H.-J.; Hu, G.; Lindsey, J. S. New J. Chem. 2017, 41, 11170–11189. DOI: 10.1039/C7NJ01892D

360.  “Genome Sequence and Composition of A Tolyporphin-Producing Cyanobacterium–Microbial Community,” Hughes, R.-A.; Zhang, Y.; Zhang, R.; Williams, P. G.; Lindsey, J. S.; Miller, E. S. Appl. Environ. Microbiol. 2017, 83, e01068-17. DOI: 10.1128/AEM.01068-17

359.   “Hydrogen Evolution Catalysis by a Sparsely Substituted Cobalt Chlorin,” Maher, A. G.; Passard, G.; Dogutan, D. K.; Halbach, R. L.; Anderson, B. L.; Gagliardi, C. J.; Taniguchi, M.; Lindsey, J. S.; Nocera, D. G. ACS Catalysis 2017, 7, 3597–3606. DOI: 10.1021/acscatal.7b00969

358.   “Synthesis and Spectral Properties of meso-Arylbacteriochlorins, Including Insights into Essential Motifs of Hydrodipyrrin Precursors,” Reddy, M. N.; Zhang, S.; Kim, H.-J.; Mass, O.; Taniguchi, M.; Lindsey, J. S. Molecules 2017, 22, 634 (32 pages). DOI: 10.3390/molecules22040634

357.   “Synthesis and photophysical characterization of bacteriochlorins equipped with integral swallowtail substituents,” Liu, Y.; Allu, S.; Reddy, M. N.; Hood, D.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. New J. Chem. 2017, 41, 4360–4376. DOI: 10.1039/C7NJ00499K

356.  “Photophysical Characterization of the Naturally Occurring Dioxobacteriochlorin Tolyporphin A and Synthetic Oxobacteriochlorin Analogues, ” Hood, D.; Niedzwiedzki, D. M.; Zhang, R.; Zhang, Y.; Dai, J.; Miller, E. S.; Bocian, D. F.; Williams, P. G.; Lindsey, J. S.; Holten, D. Photochem. Photobiol. 2017, 93, 1204–1215. DOI: 10.1111/php.12781

355.  “Synthesis, photophysics and electronic structure of oxobacteriochlorins,” Liu, M.; Chen, C.-Y.; Hood, D.; Taniguchi, M.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. New J. Chem. 2017, 41, 3732–3744. DOI: 10.1039/C6NJ04135C

354.  “Construction of the Bacteriochlorin Macrocycle with Concomitant Nazarov Cyclization To Form the Annulated Isocyclic Ring: Analogues of Bacteriochlorophyll a,” Zhang, S.; Lindsey, J. S. J. Org. Chem. 2017, 82, 2489–2504. DOI: 10.1021/acs.joc.6b02878

353.   “Multi-step excitation energy transfer engineering in genetic fusions of natural and synthetic light-harvesting proteins,” Mancini, J. A.; Kodali, G.; Jiang, J.; Reddy, K. R.; Lindsey, J. S.; Bryant, D. A.; Dutton, P. L.; Moser, C. C. J. R. Soc. Interface 14: 20160896. DOI: 10.1098/rsif.2016.0896

352.  “Northern–Southern Route to Synthetic Bacteriochlorins,” Liu, Y.; Lindsey, J. S. J. Org. Chem. 2016, 81, 11882–11897. DOI: 10.1021/acs.joc.6b02334

351.  “Photophysical Properties and Electronic Structure of Porphyrins Bearing Zero to Four meso-Phenyl Substituents: New Insights Into Seemingly Well Understood Tetrapyrroles,” Mandal, A. K.; Taniguchi, M.; Diers, J. R.; Niedzwiedzki, D. M.; Kirmaier, C.; Lindsey, J. S.; Bocian, D. F.; Holten, D. J. Phys. Chem. A 2016, 120, 9719–9731. DOI: 10.1021/acs.jpca.6b09483

350.  "Tuning the Electronic Structure and Properties of Perylene–Porphyrin–Perylene Panchromatic Absorbers," Amanpour, J.; Hu, G.; Alexy, E. J.; Mandal, A. K.; Kang, H. S.; Yuen, J. M.; Diers, J. R.; Lindsey, J. S.; Holten, D.; Bocian, D. F. J. Phys. Chem. A 2016, 120, 7434–7450. DOI: 10.1021/acs.jpca.6b06857

349.  "Photophysical comparisons of PEGylated porphyrins, chlorins and bacteriochlorins in water," Mandal, A. K.; Sahin, T.; Liu, M.; Lindsey, J. S.; Bocian, D. F.; Holten, D. New J. Chem. 2016, 40, 9648–9656. DOI: 10.1039/C6NJ02091G

348.  "Synthesis of diverse acyclic precursors to pyrroles for studies of prebiotic routes to tetrapyrrole macrocycles," Chandrashaker, V.; Ptaszek, M.; Taniguchi, M.; Lindsey, J. S. New J. Chem. 2016, 40, 8786–8808. DOI: 10.1039/C6NJ02048H

347.  "Panchromatic chromophore–tetrapyrrole light-harvesting arrays constructed from bodipy, perylene, terrylene, porphyrin, chlorin, and bacteriochlorin building blocks," Hu, G.; Liu, R.; Alexy, E. J.; Mandal, A. K.; Bocian, D. F.; Holten, D.; Lindsey, J. S. New J. Chem. 2016, 40, 8032–8052. DOI: 10.1039/C6NJ01782G

346.  "Scope and limitations of two model prebiotic routes to tetrapyrrole macrocycles," Taniguchi, M.; Deans, R. M.; Chandrashaker, V.; Ptaszek, M.; Lindsey, J. S. New J. Chem. 2016, 40, 7445–7455. DOI: 10.1039/C6NJ01423B

345.  "Bioconjugatable, PEGylated Hydroporphyrins for Photochemistry and Photomedicine. Narrow-Band, Near-Infrared-Emitting Bacteriochlorins," Zhang, N.; Jiang, J.; Liu, M.; Taniguchi, M.; Mandal, A. K.; Evans-Storms, R. B.; Pitner, J. B.; Bocian, D. F.; Holten, D.; Lindsey, J. S. New J. Chem. 2016, 40, 7750–7767. DOI: 10.1039/C6NJ01155A

344.  "Bioconjugatable, PEGylated Hydroporphyrins for Photochemistry and Photomedicine. Narrow-Band, Red-Emitting Chlorins," Liu, M.; Chen, C.-Y.; Mandal, A. K.; Chandrashaker, V.; Evans-Storms, R. B.; Pitner, J. B.; Bocian, D. F.; Holten, D.; Lindsey, J. S. New J. Chem. 2016, 40, 7721–7740. DOI: 10.1039/C6NJ01154C

343.  "Complexity in Structure-Directed Prebiotic Chemistry. Reaction Bifurcation of a β-Diketone in Tetrapyrrole Formation," Deans, R. M.; Taniguchi, M.; Chandrashaker, V.; Ptaszek, M.; Lindsey, J. S. New J. Chem. 2016, 40, 6434–6440. DOI: 10.1039/C6NJ00545D

342.  "Complexity in Structure-Directed Prebiotic Chemistry. Unexpected Compositional Richness from Competing Reactants in Tetrapyrrole Formation," Deans, R. M.; Taniguchi, M.; Chandrashaker, V.; Ptaszek, M.; Chambers, D. R.; Soares, A. R. M.; Lindsey, J. S. New J. Chem. 2016, 40, 6421–6433. DOI: 10.1039/C6NJ00543H

341.  "Synthesis and Photophysical Characteristics of 2,3,12,13-Tetraalkylbacteriochlorins," Zhang, S.; Kim, H.-J.; Tang, Q.; Yang, E.; Bocian, D. F.; Holten, D.; Lindsey, J. S. New J. Chem. 2016, 40, 5942–5956. DOI: 10.1039/C6NJ00517A

340.  "The Porphobilinogen Conundrum in Prebiotic Routes to Tetrapyrrole Macrocycles," Taniguchi, M.; Ptaszek, M.; Chandrashaker, V.; Lindsey, J. S. Orig. Life Evol. Biosph. 2017, 93–119. DOI: 10.1007/s11084-016-9506-1

339.  "Synthetic Chlorins, Possible Surrogates for Chlorophylls, Prepared by Derivatization of Porphyrins," Taniguchi, M.; Lindsey, J. S. Chem. Rev. 2017, 117, 344–535. Special issue on Light-Harvesting, 01/25/2017 DOI: 10.1021/acs.chemrev.5b00696

338.  "Paley’s Watchmaker Analogy and Prebiotic Synthetic Chemistry in Surfactant Assemblies. Formaldehyde Scavenging by Pyrroles Leading to Porphyrins as a Case Study," Alexy, E. J.; Hintz, C. W.; Hughes, H. M.; Taniguchi, M.; Lindsey, J. S. Org. Biomol. Chem. 2015, 13, 10025–10031. DOI: 10.1039/c5ob01409c

337.  "Integration of Cyanine, Merocyanine, and Styryl Dye Motifs with Synthetic Bacteriochlorins," Yang, E.; Zhang, N.; Krayer, M.; Taniguchi, M.; Diers, J. R.; Kirmaier, C.; Lindsey, J. S.; Bocian, D. F.; Holten, D. Photochem. Photobiol. 2016, 92, 111–125. DOI: 10.1111/php.12547

336.  "Complexity in Structure-Directed Prebiotic Chemistry. Effect of a Defective Competing Reactant in Tetrapyrrole Formation," Deans, R. M.; Chandrashaker, V.; Taniguchi, M.; Lindsey, J. S. New J. Chem. 2015, 39, 8273–8281. DOI: 10.1039/c5nj01474c

335.  "Self-assembled Light-Harvesting System from Chromophores in Lipid Vesicles," Sahin, T.; Harris, M. A.; Vairaprakash, P.; Niedzwiedzki, D. M.; Subramanian, V.; Shreve, A. P.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Phys. Chem. B 2015, 119, 10231–10243. DOI: 10.1021/acs.jpcb.5b04841

334.  "Synthetic Bacteriochlorins Bearing Polar Motifs (Carboxylate, Phosphonate, Ammonium and a Short PEG). Water-Solubilization, Bioconjugation, and Photophysical Properties," Jiang, J.; Yang, E.; Reddy, K. R.; Niedzwiedzki, D. M.; Kirmaier, C.; Bocian, D. F.; Holten, D.; Lindsey, J. S. New J. Chem. 2015, 39, 5694–5714. DOI: 10.1039/C5NJ00759C 

333.  "Elaboration of an Unexplored Substitution Site in Synthetic Bacteriochlorins," Zhang, N.; Reddy, K. R.; Jiang, J.; Taniguchi, M.; Sommer, R. D.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2015, 19, 887–902. DOI: 10.1142/S1088424615500534 

332.  "De Novo Synthesis of Gem-Dialkyl Chlorophyll Analogues for Probing and Emulating our Green World," Lindsey, J. S. Chem. Rev. 2015, 115, 6534–6620. DOI: 10.1021/acs.chemrev.5b00065 

331.  "Near-infrared tunable bacteriochlorins equipped for bioorthogonal labeling," Jiang, J.; Taniguchi, M.; Lindsey, J. S. New J. Chem. 2015, 39, 4534–4550. DOI: 10.1039/C5NJ00209E 

330.  "Extending the Short and Long Wavelength Limits of Bacteriochlorin Near-Infrared Absorption via Dioxo- and Bisimide-Functionalization," Vairaprakash, P.; Yang, E.; Sahin, T.; Taniguchi, M.; Krayer, M.; Diers, J. R.; Wang, A.; Niedzwiedzki, D. M.; Kirmaier, C.; Lindsey, J. S.; Bocian, D. F.; Holten, D. J. Phys. Chem. B 2015, 119, 4382–4395. DOI: 10.1021/jp512818g 

329.  "Photophysical Properties and Electronic Structure of Chlorin–Imides: Bridging the Gap Between Chlorins and Bacteriochlorins," Faries, K. M.; Diers, J. R.; Springer, J. W.; Yang, E.; Ptaszek, M.; Lahaye, D.; Krayer, M.; Taniguchi, M.; Kirmaier, C.; Lindsey, J. S.; Bocian, D. F.; Holten, D. J. Phys. Chem. B 2015, 7503–7515. DOI: 10.1021/jp511257w 

328.  "Hydrophilic Bioconjugatable trans-AB-Porphyrins and Peptide Conjugates," Sahin, T.; Vairaprakash, P.; Borbas, K. E.; Balasubramanian, T.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2015, 19, 663–678. DOI: 10.1142/S1088424615500121 

327.  "Progress Towards Synthetic Chlorins with Graded Polarity, Conjugatable Substituents, and Wavelength Tunability," Ra, D.; Gauger, K. A.; Muthukumaran, K.; Balasubramanian, T.; Chandrashaker, V.; Taniguchi, M.; Yu, Z.; Talley, D. C.; Ehudin, M.; Ptaszek, M.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2015, 19, 547–572. (Cover art for the issue containing paper 327) DOI: 10.1142/S1088424615500042 

326.  "Effects of Substituents on Synthetic Analogs of Chlorophylls. Part 4: How Formyl Group Location Dictates the Spectral Properties of Chlorophylls b, d and f," Yuen, J.; Harris, M. A.; Liu, M.; Diers, J. R.; Kirmaier, C.; Bocian, D. F.; Lindsey, J. S.; Holten, D. Photochem. Photobiol. 2015, 91, 331–342. DOI: 10.1111/php.12401 

325.  "Panchromatic Absorbers for Solar Light-Harvesting," Alexy, E. J.; Yuen, J. M.; Chandrashaker, V.; Diers, J. R.; Kirmaier, C.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Chem. Commun. 2014, 50, 14512–14515. DOI: 10.1039/C4CC06853J 

324.  "Polarity-Tunable and Wavelength-Tunable Bacteriochlorins Bearing a Single Carboxylic Acid or NHS Ester. Use in a Protein Bioconjugation Model System," Jiang, J.; Chen, C.-Y.; Zhang, N.; Vairaprakash, P.; Lindsey, J. S. New J. Chem. 2015, 39, 403–419. DOI: 10.1039/C4NJ01340A 

323.  "Enhanced Light-harvesting Capacity by Micellar Assembly of Free Accessory Chromophores and LH1-like Antennas," Harris, M. A.; Sahin, T.; Jiang, J.; Vairaprakash, P.; Parkes-Loach, P. S.; Niedzwiedzki, D. M.; Kirmaier, C.; Loach, P. A.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Photochem. Photobiol. 2014, 90, 1264–1276. DOI: 10.1111/php.12319 

322.  "Vibronic Characteristics and Spin-Density Distributions in Bacteriochlorins as Revealed by Spectroscopic Studies of 16 Isotopologues. Implications for Energy- and Electron-Transfer in Natural Photosynthesis and Artificial Solar-Energy Conversion," Diers, J. R.; Tang, Q.; Hondros, C. J.; Chen, C.-Y.; Holten, D.; Lindsey, J. S.; Bocian, D. F. J. Phys. Chem. B 2014, 118, 7520–7532. DOI: 10.1021/jp504286w 

321.  "Stable Synthetic Mono-Substituted Cationic Bacteriochlorins Mediate Selective Broad-Spectrum Photoinactivation of Drug-Resistant Pathogens at Nanomolar Concentrations," Huang, L.; Krayer, M.; Roubil, J. G. S.; Huang, Y.-Y.; Holten, D.; Lindsey, J. S.; Hamblin, M. R. J. Photochem. Photobiol. B: Biol. 2014, 141, 119–127. DOI: 10.1016/j.jphotobiol.2014.09.016 

320.  "NMR Spectral Properties of 16 Synthetic Bacteriochlorins with Site-Specific 13C or 15N Substitution," Chen, C.-Y.; Taniguchi, M.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2014, 18, 433–456. (Cover art for the issue containing paper 320) DOI: 10.1142/S1088424614500199 

319.  "Amphiphilic, Hydrophilic, or Hydrophobic Synthetic Bacteriochlorins in Biohybrid Light-Harvesting Architectures. Consideration of Molecular Designs," Jiang, J.; Reddy, K. R.; Pavan, M. P.; Lubian, E.; Harris, M. A.; Jiao, J.; Kirmaier, C.; Parkes-Loach, P. S.; Loach, P. A.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Photosyn. Res. 2014, 122, 187–202. DOI: 10.1007/s11120-014-0021-9 

318.  "Photophysical Properties and Electronic Structure of Retinylidene–Chlorin–Chalcones and Analogues," Springer, J. W.; Taniguchi, M.; Krayer, M.; Ruzié, C.; Diers, J. R.; Niedzwiedzki, D. M.; Bocian, D. F.; Lindsey, J. S.; Holten, D. Photochem. Photobiol. Sci. 2014, 13, 634–650. DOI: 10.1039/c3pp50421b 

317.  "Regioselective β-Pyrrolic Bromination of Hydrodipyrrin–Dialkylboron Complexes Facilitates Access to Synthetic Models for Chlorophyll f," Liu, M.; Ptaszek, M.; Mass, O.; Minkler, D. F.; Sommer, R. D.; Bhaumik, J.; Lindsey, J. S. New J. Chem. 2014, 38, 1717–1730. DOI: 10.1039/C3NJ01508D 

316.  "Versatile Design of Biohybrid Light-Harvesting Architectures to Tune Location, Density and Spectral Coverage of Attached Synthetic Chromophores for Enhanced Energy Capture," Harris, M. A.; Jiang, J.; Niedzwiedzki, D. M.; Jiao, J.; Taniguchi, M.; Kirmaier, C.; Loach, P. A.; Bocian, D. F.; Lindsey, J. S.; Holten, D.; Parkes-Loach, P. S. Photosyn. Res. 2014, 121, 35–48. DOI: 10.1007/s11120-014-9993-8 

315.  "Probing Electronic Communication for Efficient Light-Harvesting Functionality: Dyads Containing a Common Perylene and a Porphyrin, Chlorin, or Bacteriochlorin," Yang, E.; Wang, J.; Diers, J. R.; Niedzwiedzki, D. M.; Kirmaier, C.; Bocian, D. F.; Lindsey, J. S.; Holten, D. J. Phys. Chem. B 2014, 118, 1630–1647. DOI: 10.1021/jp411629m 

314.  "Statistical Considerations on the Formation of Circular Photosynthetic Light-Harvesting Complexes from Rhodopseudomonas palustris," Taniguchi, M.; Henry, S.; Cogdell, R. J.; Lindsey, J. S. Photosyn. Res. 2014, 121, 49–60. DOI: 10.1007/s11120-014-9975-x 

313.  "Synthesis of 24 Bacteriochlorin Isotopologues, Each Containing a Symmetrical Pair of 13C or 15N Atoms in the Inner Core of the Macrocycle," Chen, C.-Y.; Bocian, D. F.; Lindsey, J. S. J. Org. Chem. 2014, 79, 1001–1016. DOI: 10.1021/jo402488n 

312.  "Hydrophilic Tetracarboxy Bacteriochlorins for Photonics Applications," Jiang, J.; Vairaprakash, P.; Reddy, K. R.; Sahin, T.; Pavan, M. P.; Lubian, E.; Lindsey, J. S. Org. Biomol. Chem. 2014, 12, 86–103. DOI: 10.1039/C3OB41791C 

311.  "Synthesis and Photophysical Properties of Chlorins Bearing 0–4 Distinct meso-Substituents," Aravindu, K.; Kim, H.-J.; Taniguchi, M.; Dilbeck, P. L.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Photochem. Photobiol. Sci. 2013, 12, 2089–2109. DOI: 10.1039/C3PP50240F 

310.  "Integration of Multiple Chromophores with Native Photosynthetic Antennas to Enhance Solar Energy Capture and Delivery," Harris, M. A.; Parkes-Loach, P. S.; Springer, J. W.; Jiang, J.; Martin, E. C.; Qian, P.; Jiao, J.; Niedzwiedzki, D. M.; Kirmaier, C.; Olsen, J. D.; Bocian, D. F.; Holten, D.; Hunter, C. N.; Lindsey, J. S.; Loach, P. A. Chem. Sci. 2013, 4, 3924–3933. DOI: 10.1039/C3SC51518D 

309.  "Serendipitous Synthetic Entrée to Tetradehydro Analogues of Cobalamins," Deans, R. M.; Mass, O.; Diers, J. R.; Bocian, D. F.; Lindsey, J. S. New J. Chem. 2013, 37, 3964–3975. DOI: 10.1039/C3NJ00574G 

308.  "Distinct Photophysical and Electronic Characteristics of Strongly Coupled Dyads Containing a Perylene Accessory Pigment and a Porphyrin, Chlorin, or Bacteriochlorin," Wang, J.; Yang, E.; Diers, J. R.; Niedzwiedzki, D. M.; Kirmaier, C.; Bocian, D. F.; Lindsey, J. S.; Holten, D. J. Phys. Chem. B 2013, 117, 9288–9304. DOI: 10.1021/jp405004d 

307.  "Amphiphilic Chlorins and Bacteriochlorins in Micellar Environments.  Molecular Design, de novo Synthesis, and Photophysical Properties," Aravindu, K.; Mass, O.; Vairaprakash, P.; Springer, J. W.; Yang, E.; Niedzwiedzki, D. M.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Chem. Sci. 2013, 4, 3459–3477. DOI: 10.1039/C3SC51335A 

306.  "Catalytic Diversification Upon Metal Scavenging in a Prebiotic Model for Formation of Tetrapyrrole Macrocycles," Soares, A. R. M.; Anderson, D. R.; Chandrashaker, V.; Lindsey, J. S. New J. Chem. 2013, 37, 2716–2732. DOI: 10.1039/C3NJ00498H  

305.  "Enumeration of Virtual Libraries of Combinatorial Modular Macrocyclic (Bracelet, Necklace) Architectures and their Linear Counterparts," Taniguchi, M.; Du, H.; Lindsey, J. S. J. Chem. Inf. Model. 2013, 53, 2203–2216. DOI: 10.1021/ci400175f 

304.  "Synthetic Bacteriochlorins with Integral Spiro-piperidine Motifs," Reddy, K. R.; Lubian, E.; Pavan, M. P.; Kim, H.-J.; Yang, E.; Holten, D.; Lindsey, J. S. New J. Chem. 2013, 37, 1157–1173. DOI: 10.1039/C3NJ41161C 

303.  "Palette of Lipophilic Bioconjugatable Bacteriochlorins for Construction of Biohybrid Light-Harvesting Architectures," Reddy, K. R.; Jiang, J.; Krayer, M.; Harris, M. A.; Springer, J. W.; Yang, E.; Jiao, J.; Niedzwiedzki, D. M.; Pandithavidana, D.; Parkes-Loach, P. S.; Kirmaier, C.; Loach, P. A.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Chem. Sci. 2013, 4, 2036–2053. DOI: 10.1039/C3SC22317E 

302.  "Photophysical Properties and Electronic Structure of Bacteriochlorin–Chalcones with Extended Near-Infrared Absorption," Yang, E.; Ruzié, C.; Krayer, M.; Diers, J. R.; Niedzwiedzki, D. M.; Kirmaier, C.; Lindsey, J. S.; Bocian, D. F.; Holten, D. Photochem. Photobiol. 2013, 89, 586–604. DOI: 10.1111/php.12053 

301.  “Aqueous-Membrane Partitioning of ß-Substituted Porphyrins Encompassing Diverse Polarity,” Soares, A. R. M.; Thanaiah, Y.; Taniguchi, M.; Lindsey, J. S. New J. Chem. 2013, 37, 1087–1097. DOI: 10.1039/C3NJ41042K 

300.  “Expanded Combinatorial Formation of Porphyrin Macrocycles in Aqueous Solution Containing Vesicles. A Prebiotic Model,” Soares, A. R. M.; Taniguchi, M.; Chandrashaker, V.; Lindsey, J. S. New J. Chem. 2013, 37, 1073–1086. DOI: 10.1039/C3NJ41041B 

299.  “Molecular Electronic Tuning of Photosensitizers to Enhance Photodynamic Therapy: Synthetic Dicyanobacteriochlorins as a Case Study,” Yang, E.; Diers, J. R.; Huang, Y.-Y.; Hamblin, M. R.; Lindsey, J. S.; Bocian, D. F.; Holten, D. Photochem. Photobiol. 2013, 89, 605–618. DOI: 10.1111/php.12021 

298.  “Synthesis and Characterization of Lipophilic, Near-Infrared Absorbing Metallobacteriochlorins,” Sun, E.; Chen, C.-Y.; Lindsey, J. S. Chem. J. Chin. Univ. 2013, 34, 776–781. DOI: 10.7503/cjcu20120865 

297.  “Effects of Linker Torsional Constraints on the Rate of Ground-State Hole Transfer in Porphyrin Dyads,” Hondros, C. J.; Aravindu, K.; Diers, J. R.; Holten, D.; Lindsey, J. S.; Bocian, D. F. Inorg. Chem. 2012, 51, 11076–11086. DOI: 10.1021/ic301613k 

296.  “Stable Synthetic Bacteriochlorins for Photodynamic Therapy: Role of Dicyano Peripheral Groups, Central Metal Substitution (2H, Zn, Pd), and Cremophor EL Delivery,” Huang, Y.-Y.; Balasubramanian, T.; Yang, E.; Diers, J. R.; Bocian, D. F.; Lindsey, J. S.; Holten, D.; Hamblin, M. R. ChemMedChem 2012, 7, 2155–2167. DOI: 10.1002/cmdc.201200351 

295.  “Synthesis and Evaluation of Cationic Bacteriochlorin Amphiphiles with Effective in vitro Photodynamic Activity Against Cancer Cells at Low Nanomolar Concentration,” Sharma, S.; Krayer, M.; Sperandio, F. F.; Huang, L.; Huang, Y.-Y.; Holten, D.; Lindsey, J. S.; Hamblin, M. R. J. Porphyrins Phthalocyanines 2013, 17, 73–85. DOI: 10.1142/S108842461250126X 

294.  “Synthesis and Physicochemical Properties of Metallobacteriochlorins,” Chen, C.-Y.; Sun, E.; Fan, D.; Taniguchi, M.; McDowell, B. E.; Yang, E.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Inorg. Chem. 2012, 51, 9443–9464. DOI: 10.1021/ic301262k 

293.  “Competing Knorr and Fischer-Fink Pathways to pyrroles in neutral aqueous solution,” Chandrashaker, V.; Taniguchi, M.; Ptaszek, M.; Lindsey, J. S. Tetrahedron 2012, 68, 6957–6967. DOI: 10.1016/j.tet.2012.05.080 

292.  “Primordial Oil Slick and the Formation of Hydrophobic Tetrapyrrole Macrocycles,” Soares, A. R. M.; Taniguchi, M.; Chandrashaker, V.; Lindsey, J. S. Astrobiol. 2012, 12, 1055–1068. DOI: 10.1089/ast.2012.0857 

291.  "Diversity, Isomer Composition, and Design of Combinatorial Libraries of Tetrapyrrole Macrocycles," Taniguchi, M.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2012, 16, 1–13. DOI: 10.1142/S1088424612004628 

290.  "Self-organization of tetrapyrrole constituents to give a photoactive protocell," Soares, A. R. M.; Taniguchi, M.; Chandrashaker, V.; Lindsey, J. S. Chem. Sci. 2012, 3, 1963–1974. DOI: 10.1039/C2SC01120D 

289.  "Tandem Combinatorial Model for the Prebiogenesis of Diverse Tetrapyrrole Macrocycles," Taniguchi, M.; Soares, A. R. M.; Chandrashaker, V.; Lindsey, J. S. New J. Chem. 2012, 36, 1057–1069. DOI: 10.1039/C2NJ21050A 

288.  “Effects of Substituents on Synthetic Analogs of Chlorophylls. Part 3: The Distinctive Impact of Auxochromes at the 7- versus 3-Positions,” Springer, J. W.; Faries, K. M.; Diers, J. R.; Muthiah, C.; Mass, O.; Kee, H. L.; Kirmaier, C.; Lindsey, J. S.; Bocian, D. F.; Holten, D. Photochem. Photobiol. 2012, 88, 651–674. DOI: 10.1111/j.1751-1097.2012.01083.x 

287.  "A trans-AB-Bacteriochlorin Building Block," Mass, O.; Lindsey, J. S. J. Org. Chem. 2011, 76, 9478–9487. DOI: 10.1021/jo201967k 

286.  "Biohybrid Photosynthetic Antenna Complexes for Enhanced Light-Harvesting," Springer, J. W.; Parkes-Loach, P. S.; Reddy, K. R.; Krayer, M.; Jiao, J.; Lee, G. M.; Niedzwiedzki, D. M.; Harris, M. A.; Kirmaier, C.; Bocian, D. F.; Lindsey, J. S.; Holten, D.; Loach, P. A. J. Am. Chem. Soc. 2012, 134, 4589–4599. DOI: 10.1021/ja207390y 

285.  "De Novo Synthesis and Properties of Analogues of the Self-Assembling Chlorosomal Bacteriochlorophylls," Mass, O.; Pandithavidana, D. R.; Ptaszek, M.; Santiago, K.; Springer, J. W.; Jiao, J.; Tang, Q.; Kirmaier, C.; Bocian, D. F.; Holten, D.; Lindsey, J. S. New J. Chem. 2011, 35, 2671–2690. DOI: 10.1039/C1NJ20611G 

284.  "Photophysical Properties and Electronic Structure of Stable, Tunable Synthetic Bacteriochlorins: Extending the Features of Native Photosynthetic Pigments," Yang, E.; Kirmaier, C.; Krayer, M.; Taniguchi, M.; Kim, H.-J.; Diers, J. R.; Bocian, D. F.; Lindsey, J. S.; Holten, D. J. Phys. Chem. B 2011, 115, 10801–10816. DOI: 10.1021/jp205258s 

283.  "Virtual Libraries of Tetrapyrrole Macrocycles. Combinatorics, Isomers, Product Distributions, and Data Mining," Taniguchi, M.; Du, H.; Lindsey, J. S. J. Chem. Inf. Model. 2011, 51, 2233–2247. DOI: 10.1021/ci200240e 

282.  "Molecules for Charge-Based Information Storage," Lindsey, J. S.; Bocian, D. F. Acc. Chem. Res. 2011, 44, 638–650. DOI: 10.1021/ar200107x 

281.  "Encoding Isotopic Watermarks in Molecular Electronic Materials as an Anti-Counterfeiting Strategy. Application to Porphyrins for Information Storage," Lindsey, J. S.; Thamyongkit, P.; Taniguchi, M.; Bocian, D. F. J. Porphyrins Phthalocyanines 2011, 15, 505–516. DOI: 10.1142/S1088424611003458 

280.  “Synthesis and Photochemical Characterization of Stable Indium Bacteriochlorins,” Krayer, M.; Yang, E.; Kim, H.-J.; Kee, H. L.; Deans, R. M.; Sluder, C. E.; Diers, J. R.; Kirmaier, C.; Bocian, D. F.; Holten, D.; Lindsey, J. S. Inorg. Chem. 2011, 50, 4607–4618. DOI: 10.1021/ic200325d 

279. “Faile Synthesis of a B,D-Tetradehydrocorrin and Rearrangement to Bacteriochlorins,” Aravindu, K.; Krayer, M.; Kim, H.-J.; Lindsey, J. S. New J. Chem. 2011, 35, 1376–1384. DOI: 10.1039/C1NJ20027E 

278.  “Tapping the Near-Infrared Spectral Region with Bacteriochlorin Arrays,” Lindsey, J. S.; Mass, O.; Chen, C.-Y. New J. Chem. 2011, 35, 511–516. DOI: 10.1039/C0NJ00977F 

277.  “De Novo Synthesis and Photophysical Characterization of Annulated Bacteriochlorins. Mimicking and Extending the Properties of Bacteriochlorophylls,” Krayer, M.; Yang, E.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. New J. Chem. 2011, 35, 587–601. DOI: 10.1039/C0NJ00771D 

276.  “Abiotic Formation of Uroporphyrinogen and Coproporphyrinogen from Acyclic Reactants,” Lindsey, J. S.; Chandrashaker, V.; Taniguchi, M.; Ptaszek, M. New J. Chem. 2011, 35, 65–75. (Cover art for the issue containing paper 276) DOI: 10.1039/C0NJ00716A 

275.  “Structural Characteristics that Make Chlorophylls Green: Interplay of Hydrocarbon Skeleton and Substituents,” Mass, O.; Taniguchi, M.; Ptaszek, M.; Springer, J. W.; Faries, K. M.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. New J. Chem. 2011, 35, 76–88. DOI: 10.1039/C0NJ00652A 

274.  “Activation Energies for Oxidation of Porphyrin Monolayers Anchored to Au(111),” Jiao, J.; Taniguchi, M.; Lindsey, J. S.; Bocian, D. F. Langmuir 2010, 26, 15718–15721. DOI: 10.1021/la102802n 

273.  “Probing the Rate of Hole Transfer in Oxidized Porphyrin Dyads Using Thallium Hyperfine Clocks,” Diers, J. R.; Taniguchi, M.; Holten, D.; Lindsey, J. S.; Bocian, D. F. J. Am. Chem. Soc. 2010, 132, 12121–12132. DOI: 10.1021/ja105082d 

272.  “Synthesis of Oligo(p-Phenylene)-linked Dyads Containing Free Base, Zinc(II) or Thallium(III) Porphyrins for Studies in Artificial Photosynthesis,” Taniguchi, M.; Lindsey, J. S. Tetrahedron 2010, 66, 5549–5565. DOI: 10.1016/j.tet.2010.05.059 

271.  “Probing the Rate of Hole Transfer in Oxidized Synthetic Chlorin Dyads via Site-Specific ¹³C-Labeling,” Nieves-Bernier, E. J.; Taniguchi, M.; Diers, J. R.; Holten, D.; Bocian, D. F.; Lindsey, J. S. J. Org. Chem. 2010, 75, 3193–3202. (Selected as featured article) DOI: 10.1021/jo100527h 

270.  “Structural Studies of Sparsely Substituted Chlorins and Phorbines Establish Benchmarks for Changes in the Ligand Core and Framework of Chlorophyll Macrocycles,” Taniguchi, M.; Mass, O.; Boyle, P. D.; Tang, Q.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Mol. Structure 2010, 979, 27–45. DOI: 10.1016/j.molstruc.2010.05.035 

269.  “Stable Synthetic Cationic Bacteriochlorins as Selective Antimicrobial Photosensitizers,” Huang, L.; Huang, Y.-Y.; Mroz, P.; Tegos, G. P.; Zhiyentayev, T.; Sharma, S. K.; Lu, Z.; Balasubramanian, T.; Krayer, M.; Ruzié, C.; Yang, E.; Kee, H. L.; Kirmaier, C.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S.; Hamblin, M. R. Antimicrob. Agents Chemother. 2010, 54, 3834–3841. DOI: 10.1128/AAC.00125-10 

268.  “In Vitro Photodynamic Therapy and Quantitative Structure-Activity Relationship Studies with Stable Synthetic Near-Infrared-Absorbing Bacteriochlorin Photosensitizers,” Huang, Y.-Y.; Mroz, P.; Zhiyentayev, T.; Balasubramanian, T.; Ruzié, C.; Krayer, M.; Fan, D.; Borbas, K. E.; Yang, E.; Kee, H. L.; Kirmaier, C.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S.; Hamblin, M. R. J. Med. Chem. 2010, 53, 4018–4027. DOI: 10.1021/jm901908s 

267.  “De Novo Synthesis of Long-Wavelength Absorbing Chlorin-13,15-Dicarboximides,” Ptaszek, M.; Lahaye, D.; Krayer, M.; Muthiah, C.; Lindsey, J. S. J. Org. Chem. 2010, 75, 1659–1673. DOI: 10.1021/jo902649d 

266.  “Stable Synthetic Bacteriochlorins Overcome the Resistance of Melanoma to Photodynamic Therapy,” Mroz, P.; Huang, Y.-Y.; Szokalska, A.; Zhiyentayev, T.; Janjua, S.; Nifli, A.-P.; Sherwood, M. E.; Ruzié, C.; Borbas, K. E.; Fan, D.; Krayer, M.; Balasubramanian, T.; Yang, E.; Kee, H. L.; Kirmaier, C.; Diers, J. R.; Bocian, D. F.; Holten, D.; Lindsey, J. S.; Hamblin, M. R. FASEB J. 2010, 24, 3160–3170. DOI: 10.1096/fj.09-152587 

265.  “Expanded Scope of Synthetic Bacteriochlorins via Improved Acid Catalysis Conditions and Diverse Dihydrodipyrrin-Acetals,” Krayer, M.; Ptaszek, M.; Kim, H.-J.; Meneely, K. R.; Fan, D.; Secor, K.; Lindsey, J. S. J. Org. Chem. 2010, 75, 1016–1039. (Selected as featured article) DOI: 10.1021/jo9025572 

264.  “Excited-State Photodynamics of Perylene-Porphyrin Dyads.  5. Tuning Light-Harvesting Characteristics via Perylene Substituents, Connection Motif, and 3-Dimensional Architecture,” Kirmaier, C.; Song, H.-E.; Yang, E. K.; Schwartz, J. K.; Hindin, E.; Diers, J. R.; Loewe, R. S.; Tomizaki, K.-y.; Chevalier, F.; Ramos, L.; Birge, R. R.; Bocian, D. F.; Lindsey, J. S.; Holten, D. J. Phys. Chem. B 2010, 114, 14249–14264. DOI: 10.1021/jp910705q 

263.  “Linker Dependence of Energy and Hole Transfer in Neutral and Oxidized Multiporphyrin Arrays,” Song, H.-E.; Taniguchi, M.; Diers, J. R.; Kirmaier, C.; Bocian, D. F.; Lindsey, J. S.; Holten, D. J. Phys. Chem. B 2009, 113, 16483–16493. DOI: 10.1021/jp9072558 

262.  “Synthetic Routes to meso-Patterned Porphyrins,” Lindsey, J. S. Acc. Chem. Res. 2010, 43, 300–311. DOI: 10.1021/ar900212t 

261.  “Refined Syntheses of Hydrodipyrrin Precursors to Chlorin and Bacteriochlorin Building Blocks,” Krayer, M.; Balasubramanian, T.; Ruzié, C.; Ptaszek, M.; Cramer, D. L.; Taniguchi, M.; Lindsey, J. S. J. Porphyrins Phthalocyanines 2009, 13, 1098–1110. DOI: 10.1142/S1088424609001406  

260.  “Synthesis and Photochemical Properties of 12-Substituted versus 13-Substituted Chlorins,” Mass, O.; Ptaszek, M.; Taniguchi, M.; Diers, J. R.; Kee, H. L.; Bocian, D. F.; Holten, D.; Lindsey, J. S. J. Org. Chem. 2009, 74, 5276–5289. DOI: 10.1021/jo900706x 

259.  “Excited-State Energy Flow in Phenylene-Linked Multiporphyrin Arrays,” Song, H.-E.; Taniguchi, M.; Speckbacher, M.; Yu, L.; Bocian, D. F.; Lindsey, J. S.; Holten, D. J. Phys. Chem. B 2009, 113, 8011–8019. DOI: 10.1021/jp902183g 

258.  “Regioselective Bromination Tactics in the De Novo Synthesis of Chlorophyll b Analogues,” Muthiah, C.; Lahaye, D.; Taniguchi, M.; Ptaszek, M.; Lindsey, J. S. J. Org. Chem. 2009, 74, 3237–3247. (Selected as featured article and as cover art) DOI: 10.1021/jo9002954 

257.  “Fast and Robust Route to Hydroporphyrin–Chalcones with Extended Red or Near-Infrared Absorption,” Ruzié, C.; Krayer, M.; Lindsey, J. S. Org. Lett. 2009, 11, 1761–1764. DOI: 10.1021/ol900277m 

256.  “Simple Formation of an Abiotic Porphyrinogen in Aqueous Solution,” Lindsey, J. S.; Ptaszek, M.; Taniguchi, M. Orig. Life Evol. Biosph. 2009, 39, 495–515. DOI: 10.1007/s11084-009-9168-3 

255.  “Imidazole Metalloporphyrins as Photosensitizers for Photodynamic Therapy: Role of Molecular Charge, Central Metal and Hydroxyl Radical Production,” Mroz, P.; Bhaumik, J.; Dogutan, D. K.; Aly, Z.; Kamal, Z.; Khalid, L.; Kee, H. L.; Bocian, D. F.; Holten, D.; Lindsey, J. S.; Hamblin, M. R. Cancer Lett. 2009, 282, 63–76. DOI: 10.1016/j.canlet.2009.02.054 

254.  “Chlorin-Bacteriochlorin Energy-transfer Dyads as Prototypes for Near-infrared Molecular Imaging Probes: Controlling Charge-transfer and Fluorescence Properties in Polar Media,” Kee, H. L.; Diers, J. R.; Ptaszek, M.; Muthiah, C.; Fan, D.; Lindsey, J. S.; Bocian, D. F.; Holten, D. Photochem. Photobiol. 2009, 85, 909–920. DOI: 10.1111/j.1751-1097.2008.00532.x 

253.  “Solution-State Conformational Ensemble of a Hexameric Porphyrin Array Characterized Using Molecular Dynamics and X-ray Scattering,” Mardis, K. L.; Sutton, H. M.; Zuo, X.; Lindsey, J. S.; Tiede, D. M. J. Phys. Chem. A 2009, 113, 2516–2523. DOI: 10.1021/jp808318x 

252.  “Tandem Dispersion and Killing of Bacteria from a Biofilm,” Rogers, S. A.; Krayer, M.; Lindsey, J. S.; Melander, C. Org. Biomol. Chem. 2009, 7, 603–606. DOI: 10.1039/B817923A 

251.  “Probing Ground-State Hole Transfer Between Equivalent, Electrochemically Inaccessible States in Multiporphyrin Arrays using Time-Resolved Optical Spectroscopy,” Song, H.-E.; Taniguchi, M.; Kirmaier, C.; Diers, J. R.; Bocian, D. F.; Lindsey, J. S.; Holten, D. Photochem. Photobiol. 2009, 85, 693–704. DOI: 10.1111/j.1751-1097.2008.00471.x 

250.  “Determination of Ground-State Hole-Transfer Rates Between Identical Sites in Oxidized Multiporphyrin Arrays Using Time-Resolved Optical Spectroscopy,” Song, H.-E.; Kirmaier, C.; Taniguchi, M.; Diers, J. R.; Bocian, D. F.; Lindsey, J. S.; Holten, D. J. Am. Chem. Soc. 2008, 130, 15636–15648. DOI: 10.1021/ja805673m 

249.  “Energy- and Hole-Transfer Dynamics in Oxidized Porphyrin Dyads,” Song, H.-E.; Kirmaier, C.; Diers, J. R.; Lindsey, J. S.; Bocian, D. F.; Holten, D. J. Phys. Chem. B 2009, 113, 54–63. DOI: 10.1021/jp8060637 

248.  “Comparison of Electron-Transfer Rates for Metal- versus Ring-Centered Redox Processes of Porphyrins in Monolayers on Au(111),” Jiao, J.; Schmidt, I.; Taniguchi, M.; Lindsey, J. S.; Bocian, D. F. Langmuir 2008, 24, 12047–12053. DOI: 10.1021/la8019843 

247.  “Regiospecifically α-¹³C-Labeled Porphyrins for Studies of Ground-State Hole Transfer in Multiporphyrin Arrays,” Muresan, A, Z.; Thamyongkit, P.; Diers, J. R.; Holten, D.; Lindsey, J. S.; Bocian, D. F. J. Org. Chem. 2008, 73, 6947–6959. (Selected as featured article) DOI: 10.1021/jo8012836 

246.  “Design and Synthesis of Water-Soluble Bioconjugatable trans-AB-Porphyrins,” Muresan, A. Z.; Lindsey, J. S. Tetrahedron 2008, 64, 11440–11448. DOI: 10.1016/j.tet.2008.08.096 

245.  “Photophysical Characterization of Imidazolium-Substituted Pd(II), In(III), and Zn(II) Porphyrins as Photosensitizers for Photodynamic Therapy,” Kee, H. L.; Bhaumik, J.; Diers, J. R.; Mroz, P.; Hamblin, M. R.; Bocian, D. F.; Lindsey, J. S.; Holten, D. J. Photochem. Photobiol. A: Chem. 2008, 200, 346–355. DOI: 10.1016/j.jphotochem.2008.08.006 

244.  “Investigation of the Scope of a New Route to ABCD-Bilanes and ABCD-Porphyrins,” Dogutan, D. K.; Lindsey, J. S. J. Org. Chem. 2008, 73, 6728–6742. DOI: 10.1021/jo8010396  

243.  “Examination of Chlorin–Bacteriochlorin Energy-Transfer Dyads as Prototypes for Near-Infrared Molecular Imaging Probes,” Kee, H. L.; Nothdurft, R.; Muthiah, C.; Diers, J. R.; Fan, D.; Ptaszek, M.; Bocian, D. F.; Lindsey, J. S.; Culver, J. P.; Holten, D. Photochem. Photobiol. 2008, 84, 1061–1072. DOI: 10.1111/j.1751-1097.2008.00409.x