较重的不同基酸离子
Corina Stoian1, Marian Olaru1, Serhiy Demeshko2
1Institut für Anorganische Chemie und Kristallographie, Universität Bremen, Leobener Straße 7, 28359, Bremen, Germany.
研究人员合成和特征较重的diferrocenylpnictogenium离子 ([Fc2E]+,E=As,Sb,Bi),扩展了先前在diferrocenylphosphenium离子上的工作. 内分子铁协调稳定了这些易斯酸性化合物.
科学领域:
- 有机金属化学 有机金属化学
- 主群 化学 化学
- 协调化学 协调化学
背景情况:
- 不同基离子 ([Fc2P]+) 是已知的化合物.
- 将这项研究扩展到更重的菌素 (As,Sb,Bi) 是有趣的.
研究的目的:
- 为了合成和表征更重的基离子 ([Fc2E]+,E=As,Sb,Bi).
- 研究这些化合物的结构,电子和反应性质.
- 为了与更轻的diferrocenylphosphenium离子进行比较.
主要方法:
- [Fc2E]+ (E=As,Sb,Bi) 化合物的合成.
- 使用X射线晶体学和光谱学进行表征.
- 使用古特曼-贝克特法确定易斯酸度.
- 电化学氧化和还原研究.
主要成果:
- 成功合成并对[Fc2E]+ (E=P,As,Sb,Bi) 的结构性表征.
- 观察分子内铁的协调到 pnictogen 原子.
- 化合物表现出强烈的易斯酸性.
- 氧化导致二解 [Fc2E]2+ (E=P,As),还原产生中性二基因 Fc2EEFc2 (E=P,As).
结论:
- 内部分子铁协调稳定了缺电子的核酸中心.
- 合成的化合物是强大的易斯酸.
- 反应性包括形成滴度和中性滴度物质.
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