
Journal of Organometallic Chemistry p. 9 - 19 (1991)
Update date:2022-07-29
Topics:
Igarashi, Masatoshi
Ueda, Toyotoshi
Wakasa, Masanobu
Sakaguchi, Yoshio
The reaction mechanism of photo-induced electron transfer reactions from hexamethyldisilane to quinones in chloroform solution was studied at room temperature by means of a CIDNP technique.With irradiation, the formation of the corresponding mono- and di-trimethylsilylhydroquinones and trimethylsilyl chloride was confirmed by GC, GC-MS, and 1H NMR spectra.The absorptive CIDNP phase of the mono-trimethylsilyl hydroquinone indicates that this reaction precursor is the triplet radical ion pair of the hexamethyldisilane cation radical and quinone anion radical, and that the former radical reacts with the latter prior to the fission of its Si-Si bond.
View MoreBeijing ZhongDaXinHe Chemical Product Co.,Ltd(expird)
Contact:010-52876516
Address:tongzhoubeiyuan
NINGBO PANGS CHEM INT’L CO., LTD.
Contact:+86-0574-27666801
Address:Floor 21, Building 11, Xintiandi, No. 689, Shijiroad, Ningbo, Zhejiang, China
Shanghai Yurui Biotechnology(Anyang) Pharmaceutical Co., Ltd
Contact:+86-0372-3662335 +86-0372-3661988
Address:hanling industrial park anyang
website:http://www.easchem.com
Contact:+86-731-89722861 89722891
Address:2/F-4/Bld Colorful Palace, No.605 Changsha Ave, Yuhua Area Changsha Hunan China.
website:http://www.afinechem.com
Contact:+86-571-85134551
Address:No. 206 Zhen Hua Road, Hangzhou 310030, Zhejiang, China
Doi:10.1039/c2cc32176a
(2012)Doi:10.1055/s-0031-1290945
(2012)Doi:10.1021/jo00112a042
(1995)Doi:10.1002/cctc.201500142
(2015)Doi:10.1002/hc.21032
(2012)Doi:10.1016/S0040-4039(00)77667-2
(1992)