Crystal Structures
2010–2015
25 structures
Deposition Number: 1052029
Database Identifier: UYITIH
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
Deposition Number: 1029006
Database Identifier: UYIPEZ
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. DOI: 10.1142/S1088424615500042
Deposition Number: 978333
Database Identifier: VISYUT
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
Deposition Number: 974412
Database Identifier: LIXLUB
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
Deposition Number: 974411
Database Identifier: LIXLOV
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
Deposition Number: 974410
Database Identifier: LIXDON
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
Deposition Number: 974409
Database Identifier: LIXLIP
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
Deposition Number: 958397
Database Identifier: MIQHOL
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
Deposition Number: 958396
Database Identifier: MIQHUR
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
Deposition Number: 941758
Database Identifier: NIGTUU
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
Deposition Number: 919107
Database Identifier: BENRET
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
Deposition Number: 919106
Database Identifier: BENRIX
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
Deposition Number: 919105
Database Identifier: BENROD
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
Deposition Number: 881530
Database Identifier: NEJMIA
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
Deposition Number: 881529
Database Identifier: NEJMEW
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
Deposition Number: 809306
Database Identifier: OTIXUL
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
Deposition Number: 769377
Database Identifier: PACSAP
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
Deposition Number: 769376
Database Identifier: PACRUI
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
Deposition Number: 769375
Database Identifier: PACROC
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
Deposition Number: 769374
Database Identifier: PACRIW
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
Deposition Number: 769373
Database Identifier: PACRES
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
Deposition Number: 812864
Database Identifier: OKUNAK
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. DOI: 10.1021/jo9025572
Deposition Number: 812175
Database Identifier: OJOXUH
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
Deposition Number: 812174
Database Identifier: OJOXOB
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
Deposition Number: 812173
Database Identifier: OJOXIV
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