Stable Dihydrogen Complexes of Cobalt(-I) Suggest an Inverse trans-Influence of Lewis Acidic Group 13 Metalloligands

Matthew V. Vollmer; Jing Xie; Connie C. Lu

doi:10.1021/jacs.7b02870

Stable Dihydrogen Complexes of Cobalt(-I) Suggest an Inverse trans-Influence of Lewis Acidic Group 13 Metalloligands

Matthew V. Vollmer
, Jing Xie
, Connie C. Lu^*

^*此作品的通讯作者

University of Minnesota Twin Cities

科研成果: 期刊稿件 › 文章 › 同行评审

66 引用（Scopus）

摘要

A triad of d¹⁰ cobalt dihydrogen complexes was synthesized by utilizing Lewis acidic group 13 metalloligands, M[N((o-C₆H₄)NCH₂PⁱPr₂)₃], where M = Al, Ga, and In. These complexes have formal Co(-I) oxidation states, representing the only coordination complexes in which dihydrogen is bound to a subvalent transition metal center. Single-crystal X-ray diffraction and NMR studies support the assignment of these complexes as nonclassical dihydrogen adducts of Co(-I).

源语言	英语
页（从-至）	6570-6573
页数	4
期刊	Journal of the American Chemical Society
卷	139
期	19
DOI	https://doi.org/10.1021/jacs.7b02870
出版状态	已出版 - 17 5月 2017
已对外发布	是

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title = "Stable Dihydrogen Complexes of Cobalt(-I) Suggest an Inverse trans-Influence of Lewis Acidic Group 13 Metalloligands",

abstract = "A triad of d10 cobalt dihydrogen complexes was synthesized by utilizing Lewis acidic group 13 metalloligands, M[N((o-C6H4)NCH2PiPr2)3], where M = Al, Ga, and In. These complexes have formal Co(-I) oxidation states, representing the only coordination complexes in which dihydrogen is bound to a subvalent transition metal center. Single-crystal X-ray diffraction and NMR studies support the assignment of these complexes as nonclassical dihydrogen adducts of Co(-I).",

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AU - Vollmer, Matthew V.

AU - Xie, Jing

AU - Lu, Connie C.

PY - 2017/5/17

Y1 - 2017/5/17

N2 - A triad of d10 cobalt dihydrogen complexes was synthesized by utilizing Lewis acidic group 13 metalloligands, M[N((o-C6H4)NCH2PiPr2)3], where M = Al, Ga, and In. These complexes have formal Co(-I) oxidation states, representing the only coordination complexes in which dihydrogen is bound to a subvalent transition metal center. Single-crystal X-ray diffraction and NMR studies support the assignment of these complexes as nonclassical dihydrogen adducts of Co(-I).

AB - A triad of d10 cobalt dihydrogen complexes was synthesized by utilizing Lewis acidic group 13 metalloligands, M[N((o-C6H4)NCH2PiPr2)3], where M = Al, Ga, and In. These complexes have formal Co(-I) oxidation states, representing the only coordination complexes in which dihydrogen is bound to a subvalent transition metal center. Single-crystal X-ray diffraction and NMR studies support the assignment of these complexes as nonclassical dihydrogen adducts of Co(-I).

UR - https://www.scopus.com/pages/publications/85019647049

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DO - 10.1021/jacs.7b02870

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JO - Journal of the American Chemical Society

JF - Journal of the American Chemical Society

IS - 19

ER -

Stable Dihydrogen Complexes of Cobalt(-I) Suggest an Inverse trans-Influence of Lewis Acidic Group 13 Metalloligands

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