Geometric Influence on Intramolecular Photoinduced Electron Transfer in Platinum(II) Acetylide-Linked Donor-Acceptor Assemblies

被引:6
作者
Molina-Ontoria, Agustin [1 ]
Rivera-Nazario, Danisha M. [1 ]
Tigreros, Alexis [2 ]
Ortiz, Alejandro [2 ]
Nunez, Jose E. [1 ]
Insuasty, Braulio [2 ]
Lueders, Daniela [3 ]
Wolfrum, Silke [3 ]
Guldi, Dirk M. [3 ]
Echegoyen, Luis [1 ]
机构
[1] Univ Texas El Paso, Dept Chem, El Paso, TX USA
[2] Univ Valle, Dept Quim, Cali, Colombia
[3] Univ Erlangen Nurnberg, Dept Chem & Pharm, Interdisciplinary Ctr Mol Materials ICMM, D-91058 Erlangen, Germany
基金
美国国家科学基金会;
关键词
electron transfer; excited states; fullerenes; platinum(II) acetylide; triphenylamine; SENSITIZED SOLAR-CELLS; CHARGE SEPARATION; TRIPLET-STATE; BAND-GAP; COMPLEXES; POLYMERS; SYSTEMS; DESIGN; ENERGY; LUMINESCENCE;
D O I
10.1002/chem.201402616
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new donor-acceptor system, in which the electron donor triphenylamine (TPA) and the electron acceptor C-60 are bridged through a cis- or trans-platinum(II) acetylide spacer have been prepared. Ground-state studies were conducted using electrochemistry and UV/Vis spectroscopy. Fluorescence studies suggested that charge transfer is the deactivation mechanism for the singlet excited state, and this was verified by transient absorption spectroscopy. Selective photoexcitation of 1 and 2 at 387 nm leads to a fast charge transfer between the TPA and C-60, which gives rise to a radical ion-pair state (TPA(center dot+)-Pt-C-60(center dot)). Our results suggest that charge transfer is favored for the cis configuration while the presence of the trans configuration in the Pt-II diacetylide results in a longer-lived charge separated states.
引用
收藏
页码:11111 / 11119
页数:9
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