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Bis(methylene)-λ5-phosphane anions
Chemical Science ( IF 7.6 ) Pub Date : 2024-11-14 , DOI: 10.1039/d4sc07246d Akihiro Nomoto, Koh Sugamata, Takahiro Sasamori
Chemical Science ( IF 7.6 ) Pub Date : 2024-11-14 , DOI: 10.1039/d4sc07246d Akihiro Nomoto, Koh Sugamata, Takahiro Sasamori
Bis(methylene)-λ5-phosphane anions, i.e., anionic phosphorus-centered heteroallene-type molecules, were obtained from the desilylation of a bis(silyl)methyl-substituted phosphaalkene. Their molecular structures, which were determined using spectroscopic techniques and single-crystal X-ray diffraction analysis, suggest that the central di-coordinated P atom is engaged in cumulative CPC π-bonds with the neighboring C atoms. The π-bond character of the CPC moieties was examined on the basis of the experimental results in combination with theoretical calculations; the results obtained suggest that multiple silyl substitutions at the C atom weaken the CP π-bonding character.
中文翻译:
双(亚甲基)-λ5-膦阴离子
双(亚甲基)-λ5-膦阴离子,即阴离子磷中心杂丙烯型分子,是从双(硅烷基)甲基取代的磷烷基化中获得的。它们的分子结构是使用光谱技术和单晶 X 射线衍射分析确定的,表明中心双配位 P 原子与相邻的 C 原子进行累积的 C P C π键。根据实验结果结合理论计算,研究了 C P C 部分的π键特性;获得的结果表明,C 原子处的多个甲硅烷基取代削弱了 C P π键特性。
更新日期:2024-11-14
中文翻译:
双(亚甲基)-λ5-膦阴离子
双(亚甲基)-λ5-膦阴离子,即阴离子磷中心杂丙烯型分子,是从双(硅烷基)甲基取代的磷烷基化中获得的。它们的分子结构是使用光谱技术和单晶 X 射线衍射分析确定的,表明中心双配位 P 原子与相邻的 C 原子进行累积的 C P C π键。根据实验结果结合理论计算,研究了 C P C 部分的π键特性;获得的结果表明,C 原子处的多个甲硅烷基取代削弱了 C P π键特性。