Crystal Structures

2016–2019

22 structures

Deposition Number: 1934915

Database Identifier: SOQDEK

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

Deposition Number: 1934914

Database Identifier: SOQDAG

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

Deposition Number: 1900118

Database Identifier: JOBWOP

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

Deposition Number: 1900117

Database Identifier: JOBWIJ

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

Deposition Number: 1900109

Database Identifier: JOBWEF

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

Deposition Number: 1900107

Database Identifier: BOHKAN

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

Deposition Number: 1900106

Database Identifier: BOHJUG

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

Deposition Number: 1900105

Database Identifier: BOHJOA

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

Deposition Number: 1577674

Database Identifier: ADACIU

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

Deposition Number: 1530920

Database Identifier: QAXXOF

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

Deposition Number: 1530919

Database Identifier: QAXXIZ

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

Deposition Number: 1530918

Database Identifier: QAXXEV

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

Deposition Number: 1528392

Database Identifier: WAWJIQ

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

Deposition Number: 1505672

Database Identifier: ECAFUM

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

Deposition Number: 1505671

Database Identifier: ECASUZ

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

Deposition Number: 1505670

Database Identifier: ECASIN

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

Deposition Number: 1505669

Database Identifier: ECASOT

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

Deposition Number: 1488936

Database Identifier: VANYOY02

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

Deposition Number: 1488935

Database Identifier: ITUMIV

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

Deposition Number: 1488934

Database Identifier: ITUMER

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

Deposition Number: 1488933

Database Identifier: ESUCYS02

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

Deposition Number: 1453311

Database Identifier: ONILII

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