Synthesis of organoaluminum chalcogenides and their applications in Lewis acid catalysis

Yi Ding; Xiaoli Ma; Yashuai Liu; Wenqing Liu; Congjian Ni; Ben Yan; Li Yan; Zhi Yang

doi:10.1016/j.ica.2019.119091

Synthesis of organoaluminum chalcogenides and their applications in Lewis acid catalysis

Yi Ding
, Xiaoli Ma^*
, Yashuai Liu
, Wenqing Liu
, Congjian Ni
, Ben Yan
, Li Yan
, Zhi Yang

^*此作品的通讯作者

Beijing Institute of Technology

科研成果: 期刊稿件 › 文章 › 同行评审

8 引用（Scopus）

摘要

Two chalcogenide bridged bi-aluminum compounds [LAl(NMe₃)(μ-S)Al(NMe₃)L] (1) and [LAl(NMe₃)(μ-Se)Al(NMe₃)L] (2) were synthesized by reacting LAlH(NMe₃) (L = 4-methylbenzylidene-o-aminothiophenol) with one equivalent of sulfur and selenium without any catalysts in ambient temperature. Compounds 1 and 2 have been characterized by ¹H and ¹³C NMR, elemental analyses, and single crystal X-ray structural analysis. Furthermore, bi-aluminum compounds 1 or 2 were investigated as Lewis acid catalyst for the cyanosilylation of aldehydes and the condensation of aldimine and hydroboration of aldol ketones, respectively.

源语言	英语
文章编号	119091
期刊	Inorganica Chimica Acta
卷	497
DOI	https://doi.org/10.1016/j.ica.2019.119091
出版状态	已出版 - 1 11月 2019
已对外发布	是

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@article{3d4e7b72b4e34dc0b475d8041cfd3cc3,

title = "Synthesis of organoaluminum chalcogenides and their applications in Lewis acid catalysis",

abstract = "Two chalcogenide bridged bi-aluminum compounds [LAl(NMe3)(μ-S)Al(NMe3)L] (1) and [LAl(NMe3)(μ-Se)Al(NMe3)L] (2) were synthesized by reacting LAlH(NMe3) (L = 4-methylbenzylidene-o-aminothiophenol) with one equivalent of sulfur and selenium without any catalysts in ambient temperature. Compounds 1 and 2 have been characterized by 1H and 13C NMR, elemental analyses, and single crystal X-ray structural analysis. Furthermore, bi-aluminum compounds 1 or 2 were investigated as Lewis acid catalyst for the cyanosilylation of aldehydes and the condensation of aldimine and hydroboration of aldol ketones, respectively.",

keywords = "Condensation, Cyanosilylation, Lewis acid catalysis, Organoaluminum chalcogenides",

author = "Yi Ding and Xiaoli Ma and Yashuai Liu and Wenqing Liu and Congjian Ni and Ben Yan and Li Yan and Zhi Yang",

note = "Publisher Copyright: {\textcopyright} 2019 Elsevier B.V.",

year = "2019",

month = nov,

day = "1",

doi = "10.1016/j.ica.2019.119091",

language = "English",

volume = "497",

journal = "Inorganica Chimica Acta",

issn = "0020-1693",

publisher = "Elsevier B.V.",

}

TY - JOUR

T1 - Synthesis of organoaluminum chalcogenides and their applications in Lewis acid catalysis

AU - Ding, Yi

AU - Ma, Xiaoli

AU - Liu, Yashuai

AU - Liu, Wenqing

AU - Ni, Congjian

AU - Yan, Ben

AU - Yan, Li

AU - Yang, Zhi

PY - 2019/11/1

Y1 - 2019/11/1

N2 - Two chalcogenide bridged bi-aluminum compounds [LAl(NMe3)(μ-S)Al(NMe3)L] (1) and [LAl(NMe3)(μ-Se)Al(NMe3)L] (2) were synthesized by reacting LAlH(NMe3) (L = 4-methylbenzylidene-o-aminothiophenol) with one equivalent of sulfur and selenium without any catalysts in ambient temperature. Compounds 1 and 2 have been characterized by 1H and 13C NMR, elemental analyses, and single crystal X-ray structural analysis. Furthermore, bi-aluminum compounds 1 or 2 were investigated as Lewis acid catalyst for the cyanosilylation of aldehydes and the condensation of aldimine and hydroboration of aldol ketones, respectively.

AB - Two chalcogenide bridged bi-aluminum compounds [LAl(NMe3)(μ-S)Al(NMe3)L] (1) and [LAl(NMe3)(μ-Se)Al(NMe3)L] (2) were synthesized by reacting LAlH(NMe3) (L = 4-methylbenzylidene-o-aminothiophenol) with one equivalent of sulfur and selenium without any catalysts in ambient temperature. Compounds 1 and 2 have been characterized by 1H and 13C NMR, elemental analyses, and single crystal X-ray structural analysis. Furthermore, bi-aluminum compounds 1 or 2 were investigated as Lewis acid catalyst for the cyanosilylation of aldehydes and the condensation of aldimine and hydroboration of aldol ketones, respectively.

KW - Condensation

KW - Cyanosilylation

KW - Lewis acid catalysis

KW - Organoaluminum chalcogenides

UR - https://www.scopus.com/pages/publications/85071119801

U2 - 10.1016/j.ica.2019.119091

DO - 10.1016/j.ica.2019.119091

M3 - Article

AN - SCOPUS:85071119801

SN - 0020-1693

VL - 497

JO - Inorganica Chimica Acta

JF - Inorganica Chimica Acta

M1 - 119091

ER -

Synthesis of organoaluminum chalcogenides and their applications in Lewis acid catalysis

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