Efficient electron transfer across hydrogen bond interfaces by proton-coupled and -uncoupled pathways

被引:60
作者
Cheng, Tao [1 ]
Shen, Dong Xue [1 ]
Meng, Miao [1 ]
Mallick, Suman [1 ]
Cao, Lijiu [1 ]
Patmore, Nathan J. [2 ]
Zhang, Hong Li [1 ]
Zou, Shan Feng [1 ]
Chen, Huo Wen [1 ]
Qin, Yi [1 ]
Wu, Yi Yang [1 ]
Liu, Chun Y. [1 ]
机构
[1] Jinan Univ, Dept Chem, 601 Huang Pu Ave West, Guangzhou 510632, Guangdong, Peoples R China
[2] Univ Huddersfield, Dept Chem Sci, Huddersfield HD1 3DH, W Yorkshire, England
基金
中国国家自然科学基金;
关键词
AUXILIARY BASIS-SETS; DIMOLYBDENUM UNITS; CHARGE-TRANSFER; CORRELATION-ENERGY; TIME-SCALE; VALENCE; DENSITY; TRANSITION; SPECTROSCOPY; PROGRAM;
D O I
10.1038/s41467-019-09392-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Thermal electron transfer through hydrogen bonds remains largely unexplored. Here we report the study of electron transfer through amide-amide hydrogen bonded interfaces in mixed-valence complexes with covalently bonded Mo-2 units as the electron donor and acceptor. The rate constants for electron transfer through the dual hydrogen bonds across a distance of 12.5 angstrom are on the order of similar to 10(10)s(-1), as determined by optical analysis based on Marcus-Hush theory and simulation of nu(NH) vibrational band broadening, with the electron transfer efficiencies comparable to that of pi conjugated bridges. This work demonstrates that electron transfer across a hydrogen bond may proceed via the known proton-coupled pathway, as well as an overlooked proton-uncoupled pathway that does not involve proton transfer. A mechanistic switch between the two pathways can be achieved by manipulation of the strengths of electronic coupling and hydrogen bonding. The knowledge of the non-proton coupled pathway has shed light on charge and energy transport in biological systems.
引用
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页数:10
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