化学
磷化氢
电喷雾电离
星团(航天器)
齿合度
配体(生物化学)
转化(遗传学)
质谱法
核磁共振波谱
结晶学
立体化学
有机化学
晶体结构
催化作用
基因
受体
计算机科学
程序设计语言
生物化学
色谱法
作者
Liang‐Liang Yan,Vivian Wing‐Wah Yam
摘要
Stimuli-responsive structural transformation has attracted much attention for its potential to mimic the behavior of biological transformations and functions. Here, two unprecedented dodecanuclear and pentadecanuclear gold(I) sulfido clusters (denoted trans-Au12 and trans-Au15, respectively) with impressive stimuli-responsive interconversion have been obtained by taking advantage of the judiciously designed tridentate phosphine ligand Ltrans as the building block. Both UV light and temperature can be applied to trigger the structural conversions between trans-Au12 and trans-Au15. In addition, NMR, high-resolution electrospray ionization mass spectrometry, and UV-vis absorption spectroscopy have been employed to monitor the transformation process and decipher the mechanism of structural conversion. This work not only provides a paradigm to investigate photo-induced cluster-to-cluster transformation based on polydentate phosphine ligands but also offers a new direction for the construction of the stimuli-responsive materials.
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