Reviews
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
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
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
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, 52, 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
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
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
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
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
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
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
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
282. "Molecules for Charge-Based Information Storage," Lindsey, J. S.; Bocian, D. F. Acc. Chem. Res. 2011, 44, 638–650. DOI: 10.1021/ar200107x
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
262. “Synthetic Routes to meso-Patterned Porphyrins,” Lindsey, J. S. Acc. Chem. Res. 2010, 43, 300–311. DOI: 10.1021/ar900212t
123. “Probing Electronic Communication in Covalently Linked Multiporphyrin Arrays. A Guide to the Rational Design of Molecular Photonic Devices,” Holten, D.; Bocian, D. F.; Lindsey, J. S. Acc. Chem. Res. 2002, 35, 57–69. DOI: 10.1021/ar970264z
24. “A retrospective on the automation of laboratory synthetic chemistry,” Lindsey, J. S. Chemom. Intell. Lab. Syst.: Lab. Inf. Mgt. 1992, 17, 15–45. DOI: 10.1016/0169-7439(92)90025-B
20. “Self-Assembly in Synthetic Routes to Molecular Devices. Biological Principles and Chemical Perspectives: A Review,” Lindsey, J. S. New J. Chem. 1991, 15, 153–180. DOI: 10.1002/chin.199138328
