Spin-Orbit Charge-Transfer Intersystem Crossing (ISC) in Compact Electron Donor-Acceptor Dyads: ISC Mechanism and Application as Novel and Potent Photodynamic Therapy Reagents.


Journal

Chemistry (Weinheim an der Bergstrasse, Germany)
ISSN: 1521-3765
Titre abrégé: Chemistry
Pays: Germany
ID NLM: 9513783

Informations de publication

Date de publication:
22 Jan 2020
Historique:
received: 18 09 2019
revised: 25 10 2019
pubmed: 20 11 2019
medline: 12 2 2020
entrez: 20 11 2019
Statut: ppublish

Résumé

Spin-orbit charge-transfer intersystem crossing (SOCT-ISC) is useful for the preparation of heavy atom-free triplet photosensitisers (PSs). Herein, a series of perylene-Bodipy compact electron donor/acceptor dyads showing efficient SOCT-ISC is prepared. The photophysical properties of the dyads were studied with steady-state and time-resolved spectroscopies. Efficient triplet state formation (quantum yield Φ

Identifiants

pubmed: 31743947
doi: 10.1002/chem.201904306
doi:

Substances chimiques

Biocompatible Materials 0
Photosensitizing Agents 0
Solvents 0
Spin Labels 0
Singlet Oxygen 17778-80-2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1091-1102

Subventions

Organisme : National Natural Science Foundation of China
ID : 21673031, 21761142005, 21911530095
Organisme : State Key Laboratory of Fine Chemicals
ID : ZYTS201901
Organisme : Ministry of Education
ID : DUT2019TA06

Informations de copyright

© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Références

L. Shi, W. Xia, Chem. Soc. Rev. 2012, 41, 7687-7697.
J. Xuan, W. J. Xiao, Angew. Chem. Int. Ed. 2012, 51, 6828-6838;
Angew. Chem. 2012, 124, 6934-6944.
D. P. Hari, B. Koenig, Angew. Chem. Int. Ed. 2013, 52, 4734-4743;
Angew. Chem. 2013, 125, 4832-4842.
S. Fukuzumi, K. Ohkubo, Chem. Sci. 2013, 4, 561-574.
D. Ravelli, M. Fagnoni, A. Albini, Chem. Soc. Rev. 2013, 42, 97-113.
B. F. DiSalle, S. Bernhard, J. Am. Chem. Soc. 2011, 133, 11819-11821.
F. Gärtner, D. Cozzula, S. Losse, A. Boddien, G. Anilkumar, H. Junge, T. Schulz, N. Marquet, A. Spannenberg, S. Gladiali, Chem. Eur. J. 2011, 17, 6998-7006.
F. Gärtner, S. Denurra, S. Losse, A. Neubauer, A. Boddien, A. Gopinathan, A. Spannenberg, H. Junge, S. Lochbrunner, M. Blug, Chem. Eur. J. 2012, 18, 3220-3225.
R. Weijer, M. Broekgaarden, M. Kos, R. van Vught, E. A. Rauws, E. Breukink, T. M. van Gulik, G. Storm, M. Heger, J. Photochem. Photobiol. C 2015, 23, 103-131.
S. G. Awuah, Y. You, RSC Adv. 2012, 2, 11169-11183.
X. Li, S. Kolemen, J. Yoon, E. U. Akkaya, Adv. Funct. Mater. 2017, 27, 1604053.
A. Kamkaew, S. H. Lim, H. B. Lee, L. V. Kiew, L. Y. Chung, K. Burgess, Chem. Soc. Rev. 2013, 42, 77-88.
X. Li, S. Lee, J. Yoon, Chem. Soc. Rev. 2018, 47, 1174-1188.
W. Wu, X. Shao, J. Zhao, M. Wu, Adv. Sci. 2017, 4, 1700113.
T. N. Singh-Rachford, F. N. Castellano, Coord. Chem. Rev. 2010, 254, 2560-2573.
J. Zhao, S. Ji, H. Guo, RSC Adv. 2011, 1, 937-950.
F. N. Castellano, C. E. McCusker, Dalton Trans. 2015, 44, 17906-17910.
Y. L. Chen, S. W. Li, Y. Chi, Y. M. Cheng, S. C. Pu, Y. S. Yeh, P. T. Chou, ChemPhysChem 2005, 6, 2012-2017.
L. Jiao, F. Song, J. Cui, X. Peng, Chem. Commun. 2018, 54, 9198-9201.
S. Amemori, Y. Sasaki, N. Yanai, N. Kimizuka, J. Am. Chem. Soc. 2016, 138, 8702-8705.
N. Adarsh, M. Shanmugasundaram, R. R. Avirah, D. Ramaiah, Chem. Eur. J. 2012, 18, 12655-12662.
S. Ji, W. Wu, W. Wu, P. Song, K. Han, Z. Wang, S. Liu, H. Guo, J. Zhao, J. Mater. Chem. 2010, 20, 1953-1963.
S. Guo, K. Chen, R. Dong, Z. Zhang, J. Zhao, T. Lu, ACS Catal. 2018, 8, 8659-8670.
R. Lincoln, L. Kohler, S. Monro, H. Yin, M. Stephenson, R. Zong, A. Chouai, C. Dorsey, R. Hennigar, R. P. Thummel, S. A. McFarland, J. Am. Chem. Soc. 2013, 135, 17161-17175.
B. Ventura, G. Marconi, M. Bröring, R. Krüger, L. Flamigni, New J. Chem. 2009, 33, 428-438.
E. A. Weiss, M. J. Ahrens, L. E. Sinks, A. V. Gusev, M. A. Ratner, M. R. Wasielewski, J. Am. Chem. Soc. 2004, 126, 5577-5584.
M. T. Colvin, A. B. Ricks, A. M. Scott, D. T. Co, M. R. Wasielewski, J. Phys. Chem. A 2012, 116, 1923-1930.
Z. E. Dance, Q. Mi, D. W. McCamant, M. J. Ahrens, M. A. Ratner, M. R. Wasielewski, J. Phys. Chem. B 2006, 110, 25163-25173.
E. A. Weiss, M. J. Ahrens, L. E. Sinks, M. A. Ratner, M. R. Wasielewski, J. Am. Chem. Soc. 2004, 126, 9510-9511.
R. Ziessel, B. D. Allen, D. B. Rewinska, A. Harriman, Chem. Eur. J. 2009, 15, 7382-7393.
J. Zhao, W. Wu, J. Sun, S. Guo, Chem. Soc. Rev. 2013, 42, 5323-5351.
J. Zhao, K. Xu, W. Yang, Z. Wang, F. Zhong, Chem. Soc. Rev. 2015, 44, 8904-8939.
S. Hecht, J. M. Fréchet, J. Am. Chem. Soc. 2001, 123, 6959-6960.
N. J. Turro, V. Ramamurthy, J. C. Scaiano, Principles of Molecular Photochemistry: An Introduction, University Science Books, Sausalito, 2009.
M. B. Smith, J. Michl, Chem. Rev. 2010, 110, 6891-6936.
H. Sakai, R. Inaya, H. Nagashima, S. Nakamura, Y. Kobori, N. V. Tkachenko, T. Hasobe, J. Phys. Chem. Lett. 2018, 9, 3354-3360.
Z. Wang, J. Zhao, A. Barbon, A. Toffoletti, Y. Liu, Y. An, L. Xu, A. Karatay, H. G. Yaglioglu, E. A. Yildiz, J. Am. Chem. Soc. 2017, 139, 7831-7842.
Z. Wang, Y. Gao, M. Hussain, S. Kundu, V. Rane, M. Hayvali, E. A. Yildiz, J. Zhao, H. G. Yaglioglu, R. Das, Chem. Eur. J. 2018, 24, 18663-18675.
S. M. Dyar, E. A. Margulies, N. E. Horwitz, K. E. Brown, M. D. Krzyaniak, M. R. Wasielewski, J. Phys. Chem. B 2015, 119, 13560-13569.
E. M. Giacobbe, Q. Mi, M. T. Colvin, B. Cohen, C. Ramanan, A. M. Scott, S. Yeganeh, T. J. Marks, M. A. Ratner, M. R. Wasielewski, J. Am. Chem. Soc. 2009, 131, 3700-3712.
 
J. W. Verhoeven, J. Photochem. Photobiol. C 2006, 7, 40-60;
Y. Hou, X. Zhang, K. Chen, D. Liu, Z. Wang, Q. Liu, J. Zhao, A. Barbon, J. Mater. Chem. C 2019, 7, 12048-12074.
Z. E. Dance, S. M. Mickley, T. M. Wilson, A. B. Ricks, A. M. Scott, M. A. Ratner, M. R. Wasielewski, J. Phys. Chem. A 2008, 112, 4194-4201.
J. W. Verhoeven, H. J. van Ramesdonk, M. M. Groeneveld, A. C. Benniston, A. Harriman, ChemPhysChem 2005, 6, 2251-2260.
Z. E. Dance, M. J. Ahrens, A. M. Vega, A. B. Ricks, D. W. McCamant, M. A. Ratner, M. R. Wasielewski, J. Am. Chem. Soc. 2008, 130, 830-832.
E. A. Weiss, M. A. Ratner, M. R. Wasielewski, J. Phys. Chem. A 2003, 107, 3639-3647.
H. van Willigen, G. Jones, M. S. Farahat, J. Phys. Chem. 1996, 100, 3312-3316.
M. A. Filatov, S. Karuthedath, P. M. Polestshuk, H. Savoie, K. J. Flanagan, C. Sy, E. Sitte, M. Telitchko, F. Laquai, R. W. Boyle, J. Am. Chem. Soc. 2017, 139, 6282-6285.
Z. Wang, J. Zhao, Org. Lett. 2017, 19, 4492-4495.
K. Chen, W. Yang, Z. Wang, A. Iagatti, L. Bussotti, P. Foggi, W. Ji, J. Zhao, M. Di Donato, J. Phys. Chem. A 2017, 121, 7550-7564.
Y. Zhao, R. Duan, J. Zhao, C. Li, Chem. Commun. 2018, 54, 12329-12332.
M. A. Filatov, S. Karuthedath, P. M. Polestshuk, S. Callaghan, K. J. Flanagan, T. Wiesner, F. Laquai, M. O. Senge, ChemPhotoChem 2018, 2, 606-615.
X. F. Zhang, N. Feng, Chem. Asian J. 2017, 12, 2447-2456.
Z. Wang, J. Zhao, M. D. Donato, G. Mazzone, Chem. Commun. 2019, 55, 1510-1513.
X.-F. Zhang, X. Yang, B. Xu, Phys. Chem. Chem. Phys. 2017, 19, 24792-24804.
I. Gürol, M. Durmuş, V. Ahsen, T. Nyokong, Dalton Trans. 2007, 3782-3791.
A. Ogunsipe, T. Nyokong, J. Photochem. Photobiol. A 2005, 173, 211-220.
Y. Cakmak, S. Kolemen, S. Duman, Y. Dede, Y. Dolen, B. Kilic, Z. Kostereli, L. T. Yildirim, A. L. Dogan, D. Guc, E. U. Akkaya, Angew. Chem. Int. Ed. 2011, 50, 11937-11941;
Angew. Chem. 2011, 123, 12143-12147.
S. Duman, Y. Cakmak, S. Kolemen, E. U. Akkaya, Y. Dede, J. Org. Chem. 2012, 77, 4516-4527.
K.-Y. Chen, C.-C. Hsieh, Y.-M. Cheng, C.-H. Lai, P.-T. Chou, T. J. Chow, J. Phys. Chem. A 2006, 110, 12136-12144.
W. Wu, J. Sun, X. Cui, J. Zhao, J. Mater. Chem. C 2013, 1, 4577-4589.
X.-F. Zhang, X. Yang, J. Phys. Chem. B 2013, 117, 5533-5539.
C. Zhang, J. Zhao, S. Wu, Z. Wang, W. Wu, J. Ma, S. Guo, L. Huang, J. Am. Chem. Soc. 2013, 135, 10566-10578.
Z. Wang, Y. Xie, K. Xu, J. Zhao, K. D. Glusac, J. Phys. Chem. A 2015, 119, 6791-6806.
I. H. van Stokkum, D. S. Larsen, R. van Grondelle, Biochim. Biophys. Acta Bioenerg. 2004, 1657, 82-104.
J. Snellenburg, S. Laptenok, R. Seger, K. Mullen, I. Van Stokkum, J. Stat. Software 2012, 49, 1-22.
V. Markovic, D. Villamaina, I. Barabanov, L. M. Lawson Daku, E. Vauthey, Angew. Chem. 2011, 123, 7738-7740.
K. Xu, J. Zhao, E. G. Moore, J. Phys. Chem. C 2017, 121, 22665-22679.
N. J. Turro, M. H. Kleinman, E. Karatekin, Angew. Chem. Int. Ed. 2000, 39, 4436-4461;
Angew. Chem. 2000, 112, 4608-4634.
G. I. Likhtenstein, K. Ishii, S. Nakatsuji, Photochem. Photobiol. 2007, 83, 871-881.
A. Kawai, K. Shibuya, J. Photochem. Photobiol. C 2006, 7, 89-103.
A. Barbon, M. Brustolon, E. E. van Faassen, Phys. Chem. Chem. Phys. 2001, 3, 5342-5347.
S. Richert, G. Bullard, J. Rawson, P. J. Angiolillo, M. J. Therien, C. R. Timmel, J. Am. Chem. Soc. 2017, 139, 5301-5304.
S. Yamauchi, K. Takahashi, S. S. Islam, Y. Ohba, V. Tarasov, J. Phys. Chem. B 2010, 114, 14559-14563.
M. Tanabe, H. Matsuoka, Y. Ohba, S. Yamauchi, K. Sugisaki, K. Toyota, K. Sato, T. Takui, I. Goldberg, I. Saltsman, J. Phys. Chem. A 2012, 116, 9662-9673.
T. Miura, R. Tao, S. Shibata, T. Umeyama, T. Tachikawa, H. Imahori, Y. Kobori, J. Am. Chem. Soc. 2016, 138, 5879-5885.
I. R. Gould, J. A. Boiani, E. B. Gaillard, J. L. Goodman, S. Farid, J. Phys. Chem. A 2003, 107, 3515-3524.
T. Yogo, Y. Urano, A. Mizushima, H. Sunahara, T. Inoue, K. Hirose, M. Iino, K. Kikuchi, T. Nagano, Proc. Natl. Acad. Sci. USA 2008, 105, 28-32.
E. Henry, J. Hofrichter, Methods Enzymol. 1992, 210, 129-192.
S. Stoll, A. Schweiger, J. Magn. Reson. 2006, 178, 42-55.

Auteurs

Zhijia Wang (Z)

State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology, E-208 West Campus, 2 Ling Gong Rd., Dalian, 116024, P.R. China.

Mikhail Ivanov (M)

International Tomography Center, SB RAS Institutskaya Str. 3A, and Novosibirsk State University, Pirogova str. 2, 630090, Novosibirsk, Russia.

Yuting Gao (Y)

National Engineering Research Center for Nanomedicine, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, 430074, P.R. China.

Laura Bussotti (L)

LENS (European Laboratory for Non-Linear Spectroscopy), via N. Carrara 1, 50019, Sesto Fiorentino (FI), Italy.

Paolo Foggi (P)

LENS (European Laboratory for Non-Linear Spectroscopy), via N. Carrara 1, 50019, Sesto Fiorentino (FI), Italy.
Dipartimento di Chimica, Universita di Perugia, via Elce di Sotto 8, 06123, Perugia, Italy.

Huimin Zhang (H)

National Engineering Research Center for Nanomedicine, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, 430074, P.R. China.

Nino Russo (N)

Dipartimento di Chimica e Tecnologie Chimiche, Università della Calabria, 87036, Arcavacata di, Rende, Italy.

Bernhard Dick (B)

Lehrstuhl für Physikalische Chemie, Institut für Physikalische und Theoretische Chemie, Universität Regensburg, Universitätsstrasse 31, 93053, Regensburg, Germany.

Jianzhang Zhao (J)

State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology, E-208 West Campus, 2 Ling Gong Rd., Dalian, 116024, P.R. China.

Mariangela Di Donato (M)

LENS (European Laboratory for Non-Linear Spectroscopy), via N. Carrara 1, 50019, Sesto Fiorentino (FI), Italy.
INO, Istituto Nazionale di Ottica, Largo Enrico Fermi 6, 50125, Florence, Italy.

Gloria Mazzone (G)

Dipartimento di Chimica e Tecnologie Chimiche, Università della Calabria, 87036, Arcavacata di, Rende, Italy.

Liang Luo (L)

National Engineering Research Center for Nanomedicine, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, 430074, P.R. China.

Matvey Fedin (M)

International Tomography Center, SB RAS Institutskaya Str. 3A, and Novosibirsk State University, Pirogova str. 2, 630090, Novosibirsk, Russia.

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