Dyads with tunable near-infrared donor–acceptor excited-state energy gaps: molecular design and Förster analysis for ultrafast energy transfer

Haoyu Jing, Nikki Cecil M. Magdaong, James R. Diers, Christine Kirmaier, David F. Bocian, Dewey Holten and Jonathan S. Lindsey

Phys. Chem. Chem. Phys., 2023, 25, 1827
DOI: 10.1039/D2CP04689J

Synthesis of tailored hydrodipyrrins and their examination in directed routes to bacteriochlorins and tetradehydrocorrins

Shaofei Zhang, Muthyala Nagarjuna Reddy, Olga Mass, Han-Je Kim, Gongfang Hu and Jonathan S. Lindsey

New J. Chem., 2017, 41, 11170
DOI: 10.1039/C7NJ01892D

Annulated bacteriochlorins for near-infrared photophysical studies

Hikaru Fujita, Haoyu Jing, Michael Krayer, Srinivasarao Allu, Gorre Veeraraghavaiah, Zhiyuan Wu, Jianbing Jiang, James R. Diers, Nikki Cecil M. Magdaong, Amit K. Mandal, Arpita Roy, Dariusz M. Niedzwiedzki, Christine Kirmaier, David F. Bocian, Dewey Holten and Jonathan S. Lindsey

New J. Chem., 2019, 43, 7209
DOI: 10.1039/C9NJ01113G

Photophysical comparisons of PEGylated porphyrins, chlorins and bacteriochlorins in water

Amit Kumar Mandal, Tuba Sahin, Mengran Liu, Jonathan S. Lindsey, David F. Bocian and Dewey Holten

New J. Chem., 2016, 40, 9648
DOI: 10.1039/C6NJ02091G

Synthesis of bacteriochlorins bearing diverse β-substituents

Haoyu Jing, Pengzhi Wang, Boyang Chen, Jianbing Jiang, Pothiappan Vairaprakash, Sijia Liu, Jie Rong, Chih-Yuan Chen, Phattananawee Nalaoh and Jonathan S. Lindsey

New J. Chem., 2022, 46, 5534
DOI: 10.1039/D1NJ05852E

Total synthesis campaigns toward chlorophylls and related natural hydroporphyrins – diverse macrocycles, unrealized opportunities

Yizhou Liu, Shaofei Zhang and Jonathan S. Lindsey

Nat. Prod. Rep., 2018, 35, 879
DOI: 10.1039/C8NP00020D

Meso bromination and derivatization of synthetic bacteriochlorins

Haoyu Jing, Sijia Liu, Jianbing Jiang, Vy-Phuong Tran, Jie Rong, Pengzhi Wang and Jonathan S. Lindsey

New J. Chem., 2022, 46, 5556
DOI: 10.1039/D1NJ05853C

De Novo Synthesis of Bacteriochlorins Bearing Four Trideuteriomethyl Groups

Haoyu Jing, Qun Tang, David F. Bocian and Jonathan S. Lindsey

Organics, 2022, 3, 22
DOI: 10.3390/org3010002

Riley Oxidation of Heterocyclic Intermediates on Paths to Hydroporphyrins—A Review

Pengzhi Wang and Jonathan S. Lindsey

Molecules, 2020, 25, 1858
DOI: 10.3390/molecules25081858

Syntheses and Properties of Metalated Tetradehydrocorrins

Rui Sun, Mengran Liu, Pengzhi Wang, Yangzhong Qin, Christoph Schnedermann, Andrew G. Maher, Shao-Liang Zheng, Sijia Liu, Boyang Chen, Shaofei Zhang, Dilek K. Dogutan, Jonathan S. Lindsey and Daniel G. Nocera

Inorg. Chem., 2022, 61, 12308
DOI: 10.1021/acs.inorgchem.2c01642

Bacteriochlorin syntheses - Status, problems, and exploration

Vy-Phuong Tran, Pengzhi Wang, Nobuyuki Matsumoto, Sijia Liu, Haoyu Jing, Phattananawee Nalaoh, Khiem Chau Nguyen, Masahiko Taniguchi and Jonathan S. Lindsey

J. Porphyrins Phthalocyanines, 2023, 27, 1502
DOI: 10.1142/S1088424623501171

Structural and Photophysical Characterization of All Five Constitutional Isomers of the Octaethyl‐β,β′‐dioxo‐bacterio‐ and ‐isobacteriochlorin Series

Christian Brückner, Nivedita Chaudhri, Dustin E. Nevonen, Sayantan Bhattacharya, Arthur Graf, Elizabeth Kaesmann, Ruoshi Li, Matthew J. Guberman‐Pfeffer, Tomoyasu Mani, Arunpatcha Nimthong‐Roldán, Matthias Zeller, Adrien A. P. Chauvet and Victor Nemykin

Chemistry A European J, 2021, 27, 16189
DOI: 10.1002/chem.202103014

Structural features of 11 synthetic bacteriochlorins — comparisons with chlorins and porphyrins

Vy-Phuong Tran, Masahiko Taniguchi, Roger D. Sommer, Paul D. Boyle, Phattananawee Nalaoh and Jonathan S. Lindsey

J. Porphyrins Phthalocyanines, 2025, 29, 981
DOI: 10.1142/S1088424625500786

Photophysical Properties and Electronic Structure of Porphyrins Bearing Zero to Four meso-Phenyl Substituents: New Insights into Seemingly Well Understood Tetrapyrroles

Amit Kumar Mandal, Masahiko Taniguchi, James R. Diers, Dariusz M. Niedzwiedzki, Christine Kirmaier, Jonathan S. Lindsey, David F. Bocian and Dewey Holten

J. Phys. Chem. A, 2016, 120, 9719
DOI: 10.1021/acs.jpca.6b09483

Northern–Southern Route to Synthetic Bacteriochlorins

Yizhou Liu and Jonathan S. Lindsey

J. Org. Chem., 2016, 81, 11882
DOI: 10.1021/acs.joc.6b02334

Stepwise Reduction of Octaethyl-β,β′-dioxochlorin Isomers: Access to Structurally and Electronically Diverse Hydroporphyrins

Nivedita Chaudhri, Matthias Zeller and Christian Brückner

J. Org. Chem., 2020, 85, 13951
DOI: 10.1021/acs.joc.0c01989

Bacteriochlorin‐bis(spermine) conjugate affords an effective photodynamic action to eradicate microorganisms

María B. Ballatore, María E. Milanesio, Hikaru Fujita, Jonathan S. Lindsey and Edgardo N. Durantini

Journal of Biophotonics, 2020, 13
DOI: 10.1002/jbio.201960061

Construction of the Bacteriochlorin Macrocycle with Concomitant Nazarov Cyclization To Form the Annulated Isocyclic Ring: Analogues of Bacteriochlorophyll a

Shaofei Zhang and Jonathan S. Lindsey

J. Org. Chem., 2017, 82, 2489
DOI: 10.1021/acs.joc.6b02878

Synthesis and Spectral Properties of meso-Arylbacteriochlorins, Including Insights into Essential Motifs of their Hydrodipyrrin Precursors

Muthyala Reddy, Shaofei Zhang, Han-Je Kim, Olga Mass, Masahiko Taniguchi and Jonathan Lindsey

Molecules, 2017, 22, 634
DOI: 10.3390/molecules22040634

Origins of the Electronic Modulations of Bacterio- and Isobacteriodilactone Regioisomers

Matthew J. Guberman-Pfeffer, Remy F. Lalisse, Nisansala Hewage, Christian Brückner and José A. Gascón

J. Phys. Chem. A, 2019, 123, 7470
DOI: 10.1021/acs.jpca.9b05656

Dihydrooxazine Byproduct of a McMurry–Melton Reaction en Route to a Synthetic Bacteriochlorin

Vy-Phuong Tran, Nobuyuki Matsumoto, Phattananawee Nalaoh, Haoyu Jing, Chih-Yuan Chen and Jonathan S. Lindsey

Organics, 2022, 3, 262
DOI: 10.3390/org3030019