锁定水分子通过三元O-HO内部分子键在perhydroxylated-closo-dodecaborate中
Yanrong Jiang1,2, Zhubin Hu2, Cheng Zhong3
1Center for Transformative Science, ShanghaiTech University, Shanghai 201210, China. pengpeng@shanghaitech.edu.cn.
超基化密二甲酸B12 ((OH) 12^2-通过分子内键形成独特的水集群,从而在凝结相应用中提高稳定性和选择性.
科学领域:
- * 无机化学 无机化学
- * 物理化学 物理化学
- * 计算化学 计算机化学
背景情况:
- * 在凝结相应用中,氧化密二甲酸盐 (B12(OH) 12^2-) 的水方向选择性至关重要.
- * 了解团和水分子之间的相互作用是设计新材料的关键.
研究的目的:
- * 为了比较B12H12^2-,B12H11OH^2-,和B12(OH) 12^2-.周围的水群的结构演变.
- *阐明这些系统中水方向选择性的机制.
主要方法:
- * 直接比较水集群结构演变 (单体到六体).
- *利用了多种理论方法,包括水溶解和ab initio分子动力学.
- *分析了结模式和集群生长.
主要成果:
- * B12(OH) 12^2-将水分子锁定成分子内B-O-H三元环.
- * B-(H-O) H-O 相互作用在 B12(OH) 12^2-. 的水-键 (OH-O) 上占主导地位.
- *比B12H12^2-和B12H11OH^2-.相比,更大的,热力学稳定的水群在B12(OH) 12^2-周围形成.
结论:
- * 确定了B12 (OH) 12^2-.的新型水生长模式.
- *这些发现为设计基基组修饰的酸盐提供了基础.
- * 对冷凝相化学中的各种应用的潜在影响.
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