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
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