化学
晶体结构
碳酸氢盐
钙
离子键合
无机化学
离子
结晶学
三角晶系
Crystal(编程语言)
极化(电化学)
氢键
晶体生长
作者
Kangren Kong,Guohong Cai,Zaiqiang Ma,Yinlin Shen,Biao Jin,Pohua Chen,Yu Yin,Junliang Sun,Zhaoming Liu,Ruikang Tang
摘要
Bicarbonate reactions, especially those involving calcium, play prominent roles in the carbon cycle and biochemical processes, contributing to the largest carbon pool on Earth. However, although they were hypothesized over two centuries ago, all attempts to isolate calcium bicarbonate Ca(HCO3)2, both in nature and in the laboratory, as well as other bicarbonates of multivalent metals as pure compounds, have failed and invariably resulted in the formation of carbonates. In this study, we synthesized Ca(HCO3)2 crystals by modifying the bonding environment to increase the stability of the bicarbonate ions and determined their crystal structure. Ca(HCO3)2 crystals with direct calcium–bicarbonate bonds share an identical rhombohedral crystal structure with calcite. We further determined that the polarization of calcium-bonded bicarbonate ions in polarization-favorable environments (e.g., water solvation) inhibits the isolation of Ca(HCO3)2, as it polarizes the hydroxy group to destabilize the calcium–bicarbonate ion pairing, which is a prerequisite for Ca(HCO3)2 crystallization. These findings, particularly the first-ever resolved crystal structure of Ca(HCO3)2, provide fundamental insight into metal–bicarbonate interactions and the formation of ionic compounds, advancing the ability to direct CO2-involved reactions.
科研通智能强力驱动
Strongly Powered by AbleSci AI