A long-lived charge-separated state of spiro compact electron donor-acceptor dyads based on rhodamine and naphthalenediimide chromophores

被引:11
|
作者
Xiao, Xiao [1 ]
Kurganskii, Ivan [2 ,3 ]
Maity, Partha [4 ]
Zhao, Jianzhang [1 ,5 ]
Jiang, Xiao [6 ]
Mohammed, Omar F. [4 ]
Fedin, Matvey [2 ,3 ]
机构
[1] Dalian Univ Technol, Frontiers Sci Ctr Smart Mat, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] RAS, Int Tomog Ctr, SB, Institutskaya Str 3A, Novosibirsk 630090, Russia
[3] NovosibirskState Univ, Pirogova Str 2, Novosibirsk 630090, Russia
[4] King Abdullah Univ Sci & Technol KAUST, Div Phys Sci & Engn, Thuwal 239556900, Saudi Arabia
[5] Xinjiang Univ, Coll Chem, State Key Lab Chem & Utilizat Carbon Based Energy, Urumqi 830017, Peoples R China
[6] NovosibirskState Univ, Key Lab Ind Ecol & Environm Engn, Sch Environm Sci & Technol, Minist Educ, Pirogova Str 2, Novosibirsk 630090, Russia
关键词
RADICAL-ION PAIRS; TRANSITION-METAL-COMPLEXES; EXCITED-STATE; TRIPLET-STATES; RECOMBINATION; DYNAMICS; DESIGN; DEPENDENCE; PERYLENE; ENERGY;
D O I
10.1039/d2sc04258d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Spiro rhodamine (Rho)-naphthalenediimide (NDI) electron donor-acceptor orthogonal dyads were prepared to generate a long-lived charge separation (CS) state based on the electron spin control approach, i.e. to form the (CS)-C-3 state, not the (CS)-C-1 state, to prolong the CS state lifetime by the electron spin forbidden feature of the charge recombination process of (CS)-C-3 -> S-0. The electron donor Rho (lactam form) is attached via three sigma bonds, including two C-C and one N-N bonds (Rho-NDI), or an intervening phenylene, to the electron acceptor NDI (Rho-Ph-NDI and Rho-PhMe-NDI). Transient absorption (TA) spectra show that fast intersystem crossing (ISC) (< 120 fs) occurred to generate an upper triplet state localized on the NDI moiety ((NDI)-N-3*), and then to form the CS state. For Rho-NDI in both non-polar and polar solvents, a long-lived (CS)-C-3 state (lifetime tau = 0.13 mu s) and charge separation quantum yield (phi(CS)) up to 25% were observed, whereas for Rho-Ph-NDI (tau(T) = 1.1 mu s) and Rho-PhMe-NDI (tau(T) = 2.0 mu s), a low-lying (NDI)-N-3* state was formed by charge recombination (CR) in n-hexane (HEX). In toluene (TOL), however, CS states were observed for Rho-Ph-NDI (0.37 mu s) and Rho-PhMe-NDI (0.63 mu s). With electron paramagnetic resonance (EPR) spectra, weak electronic coupling between the Rho and NDI moieties for Rho-NDI was proved. Time-resolved EPR (TREPR) spectra detected two transient species including NDI-localized triplets (formed via SOC-ISC) and a (CS)-C-3 state. The CS state of Rho-NDI features the largest dipolar interaction (|D| = 184 MHz) compared to Rho-Ph-NDI (|D| = 39 MHz) and Rho-PhMe-NDI (|D| = 41 MHz) due to the smallest distance between Rho and NDI moieties. For Rho-NDI, the time-dependent e,a & RARR; a,e phase change of the CS state TREPR spectrum indicates that the long-lived CS state is based on the electron spin control effect.
引用
收藏
页码:13426 / 13441
页数:16
相关论文
共 50 条
  • [1] Long-lived triplet charge-separated state in naphthalenediimide based donor-acceptor systems
    Aster, Alexander
    Rumble, Christopher
    Bornhof, Anna-Bea
    Huang, Hsin-Hua
    Sakai, Naomi
    Solomek, Tomas
    Matile, Stefan
    Vauthey, Eric
    [J]. CHEMICAL SCIENCE, 2021, 12 (13) : 4908 - 4915
  • [2] Long-lived charge-separated states of simple electron donor-acceptor dyads using porphyrins and phthalocyanines
    Ohkubo, Kei
    Fukuzumi, Shunichi
    [J]. JOURNAL OF PORPHYRINS AND PHTHALOCYANINES, 2008, 12 (09) : 993 - 1004
  • [3] Long-Lived Charge-Separated State in Naphthalimide-Phenothiazine Compact Electron Donor-Acceptor Dyads: Effect of Molecular Conformation Restriction and Solvent Polarity
    Xiao, Xiao
    Yan, Yuxin
    Sukhanov, Andrey A.
    Doria, Sandra
    Iagatti, Alessandro
    Bussotti, Laura
    Zhao, Jianzhang
    Di Donato, Mariangela
    Voronkova, Violeta K.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2023, 127 (31): : 6982 - 6998
  • [4] A small cationic donor-acceptor iridium complex with a long-lived charge-separated state
    Geiss, Barbara
    Lambert, Christoph
    [J]. CHEMICAL COMMUNICATIONS, 2009, (13) : 1670 - 1672
  • [5] Long-Lived Charge-Transfer State in Spiro Compact Electron Donor-Acceptor Dyads Based on Pyromellitimide-Derived Rhodamine: Charge Transfer Dynamics and Electron Spin Polarization
    Chen, Xi
    Sukhanov, Andrey A.
    Yan, Yuxin
    Bese, Damla
    Bese, Cagri
    Zhao, Jianzhang
    Voronkova, Violeta K.
    Barbon, Antonio
    Yaglioglu, Halime Gul
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2022, 61 (33)
  • [6] Fullerene acting as an electron donor in a donor-acceptor dyad to attain the long-lived charge-separated state by complexation with scandium ion
    Ohkubo, Kei
    Ortiz, Javier
    Martin-Gomis, Luis
    Fernandez-Lazaro, Fernando
    Sastre-Santos, Angela
    Fukuzumi, Shunichi
    [J]. CHEMICAL COMMUNICATIONS, 2007, (06) : 589 - 591
  • [7] Long-lived charge-transfer states in compact donor-acceptor dyads
    Verhoeven, JW
    van Ramesdonk, HJ
    Groeneveld, MM
    Benniston, AC
    Harriman, A
    [J]. CHEMPHYSCHEM, 2005, 6 (11) : 2251 - 2260
  • [8] Long-lived charge separated state and thermally activated delayed fluorescence in anthraquinone-phenoxazine electron donor-acceptor dyads
    Zhao, Xiaoyu
    Zhao, Jianzhang
    [J]. CHEMICAL COMMUNICATIONS, 2022, 58 (55) : 7666 - 7669
  • [9] A new rhenium(I) tricarbonylpolypyridine donor-acceptor complex featuring a long-lived charge-separated excited state
    Ziessel, R
    Juris, A
    Venturi, M
    [J]. CHEMICAL COMMUNICATIONS, 1997, (17) : 1593 - 1594
  • [10] Long-lived charge-separated states following excitation of Cu(I) donor-acceptor compounds
    Ruthkosky, M
    Kelly, CA
    Zaros, MC
    Meyer, GJ
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (49) : 12004 - 12005