An acyclic zincagermylene: Rapid activation of dihydrogen at sub-ambient temperature

Martin M. Juckel; Jamie Hicks; Dandan Jiang; Lili Zhao; Gernot Frenking; Cameron Jones

doi:10.1039/c7cc08430g

An acyclic zincagermylene: Rapid activation of dihydrogen at sub-ambient temperature

Martin M. Juckel, Jamie Hicks, Dandan Jiang, Lili Zhao, Gernot Frenking, Cameron Jones

化学与分子工程学院

科研成果: 期刊稿件 › 文章 › 同行评审

37 引用（Scopus）

摘要

The first example of a stable zincagermylene,:Ge(TBoN)(ZnL∗) (TBoN = N(SiMe₃){B(DipNCH)₂}, Dip = C₆H₃Prⁱ₂-2,6; L∗ = -N{C₆H₂[C(H)Ph₂]₂Me-2,6,4}(SiPrⁱ₃)) is prepared and shown to have unprecedented reactivity for a germylene, with respect to the activation of dihydrogen. Computational analyses point towards this being partially derived from the electron releasing nature of the amido-zinc fragment, which leads to a narrowing of the HOMO-LUMO gap in the compound.

源语言	英语
页（从-至）	12692-12695
页数	4
期刊	Chemical Communications
卷	53
期	94
DOI	https://doi.org/10.1039/c7cc08430g
出版状态	已出版 - 2017

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abstract = "The first example of a stable zincagermylene,:Ge(TBoN)(ZnL∗) (TBoN = N(SiMe3){B(DipNCH)2}, Dip = C6H3Pri2-2,6; L∗ = -N{C6H2[C(H)Ph2]2Me-2,6,4}(SiPri3)) is prepared and shown to have unprecedented reactivity for a germylene, with respect to the activation of dihydrogen. Computational analyses point towards this being partially derived from the electron releasing nature of the amido-zinc fragment, which leads to a narrowing of the HOMO-LUMO gap in the compound.",

author = "Juckel, {Martin M.} and Jamie Hicks and Dandan Jiang and Lili Zhao and Gernot Frenking and Cameron Jones",

note = "Publisher Copyright: {\textcopyright} 2017 The Royal Society of Chemistry.",

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doi = "10.1039/c7cc08430g",

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T1 - An acyclic zincagermylene

T2 - Rapid activation of dihydrogen at sub-ambient temperature

AU - Juckel, Martin M.

AU - Hicks, Jamie

AU - Jiang, Dandan

AU - Zhao, Lili

AU - Frenking, Gernot

AU - Jones, Cameron

PY - 2017

Y1 - 2017

N2 - The first example of a stable zincagermylene,:Ge(TBoN)(ZnL∗) (TBoN = N(SiMe3){B(DipNCH)2}, Dip = C6H3Pri2-2,6; L∗ = -N{C6H2[C(H)Ph2]2Me-2,6,4}(SiPri3)) is prepared and shown to have unprecedented reactivity for a germylene, with respect to the activation of dihydrogen. Computational analyses point towards this being partially derived from the electron releasing nature of the amido-zinc fragment, which leads to a narrowing of the HOMO-LUMO gap in the compound.

AB - The first example of a stable zincagermylene,:Ge(TBoN)(ZnL∗) (TBoN = N(SiMe3){B(DipNCH)2}, Dip = C6H3Pri2-2,6; L∗ = -N{C6H2[C(H)Ph2]2Me-2,6,4}(SiPri3)) is prepared and shown to have unprecedented reactivity for a germylene, with respect to the activation of dihydrogen. Computational analyses point towards this being partially derived from the electron releasing nature of the amido-zinc fragment, which leads to a narrowing of the HOMO-LUMO gap in the compound.

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DO - 10.1039/c7cc08430g

M3 - 文章

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AN - SCOPUS:85035129293

SN - 1359-7345

VL - 53

SP - 12692

EP - 12695

JO - Chemical Communications

JF - Chemical Communications

IS - 94

ER -

An acyclic zincagermylene: Rapid activation of dihydrogen at sub-ambient temperature

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