A multimiclear coordination system of L-cysteine and L-penicillamine that induce opposite chiralities at metal centers

Yuko Sameshima; Nobuto Yoshinari; Kiyoshi Tsuge; Asako Igashira-Kamiyama; Takumi Konno

doi:10.1002/anie.200904635

A multimiclear coordination system of L-cysteine and L-penicillamine that induce opposite chiralities at metal centers

Yuko Sameshima, Nobuto Yoshinari, Kiyoshi Tsuge, Asako Igashira-Kamiyama, Takumi Konno^*

^*この論文の責任著者

化学科

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

43 被引用数 (Scopus)

抄録

L-penicillamine (L-pen) ligands are incorporated in similar pentanuclear Au'₃M₂ (M = Ni¹¹, Co¹¹¹) structures with, however, opposite stereochemical configurations. This phenomenon is explained in terms of intramolecular hydrogen bonding and steric interactions, which may provide insight into why D-penicillamine behaves like L-cysteine in nature.

本文言語	英語
ページ（範囲）	8469-8472
ページ数	4
ジャーナル	Angewandte Chemie - International Edition
巻	48
号	45
DOI	https://doi.org/10.1002/anie.200904635
出版ステータス	出版済み - 2009/10/26

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10.1002/anie.200904635

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title = "A multimiclear coordination system of L-cysteine and L-penicillamine that induce opposite chiralities at metal centers",

abstract = "L-penicillamine (L-pen) ligands are incorporated in similar pentanuclear Au'3M2 (M = Ni11, Co111) structures with, however, opposite stereochemical configurations. This phenomenon is explained in terms of intramolecular hydrogen bonding and steric interactions, which may provide insight into why D-penicillamine behaves like L-cysteine in nature.",

keywords = "Amino acids, Chirality, Coordination modes, S ligands, Transition metals",

author = "Yuko Sameshima and Nobuto Yoshinari and Kiyoshi Tsuge and Asako Igashira-Kamiyama and Takumi Konno",

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T1 - A multimiclear coordination system of L-cysteine and L-penicillamine that induce opposite chiralities at metal centers

AU - Sameshima, Yuko

AU - Yoshinari, Nobuto

AU - Tsuge, Kiyoshi

AU - Igashira-Kamiyama, Asako

AU - Konno, Takumi

PY - 2009/10/26

Y1 - 2009/10/26

N2 - L-penicillamine (L-pen) ligands are incorporated in similar pentanuclear Au'3M2 (M = Ni11, Co111) structures with, however, opposite stereochemical configurations. This phenomenon is explained in terms of intramolecular hydrogen bonding and steric interactions, which may provide insight into why D-penicillamine behaves like L-cysteine in nature.

AB - L-penicillamine (L-pen) ligands are incorporated in similar pentanuclear Au'3M2 (M = Ni11, Co111) structures with, however, opposite stereochemical configurations. This phenomenon is explained in terms of intramolecular hydrogen bonding and steric interactions, which may provide insight into why D-penicillamine behaves like L-cysteine in nature.

KW - Amino acids

KW - Chirality

KW - Coordination modes

KW - S ligands

KW - Transition metals

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U2 - 10.1002/anie.200904635

DO - 10.1002/anie.200904635

M3 - 学術論文

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AN - SCOPUS:70350304148

SN - 1433-7851

VL - 48

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JO - Angewandte Chemie - International Edition

JF - Angewandte Chemie - International Edition

IS - 45

ER -

A multimiclear coordination system of L-cysteine and L-penicillamine that induce opposite chiralities at metal centers

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