Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing 100084, People's Republic of China.
J Am Chem Soc. 2009 Sep 23;131(37):13490-7. doi: 10.1021/ja905032g.
Complexation of cationic 5,10,15,20-tetrakis(1-methyl-4-pyridinio)porphyrin (TMPyP) and negatively charged chemically converted graphene (CCG) sheets was performed by simply mixing the diluted aqueous solutions of both components. During this process, a large bathochromic shift of porphyrin Soret band from 421 to 458 nm was observed, which is attributed to the flattening of TMPyP molecules induced by CCG through electrostatic and pi-pi stacking cooperative interactions. Furthermore, the coordination reaction between TMPyP and Cd(2+) ions was greatly accelerated from 20 h to 8 min under ambient conditions by introducing CCG sheets. On the basis of this phenomenon, we used the complex of TMPyP and CCG as an optical probe for rapid and selective detection of Cd(2+) ions in aqueous media.
将阳离子 5,10,15,20-四(1-甲基-4-吡啶基)卟啉(TMPyP)和带负电荷的化学转化石墨烯(CCG)片通过简单混合两种成分的稀释水溶液进行复合。在这个过程中,卟啉 Soret 带从 421nm 发生了很大的红移到 458nm,这归因于 CCG 通过静电和 π-π 堆积协同相互作用诱导 TMPyP 分子的变平。此外,通过引入 CCG 片,TMPyP 与 Cd(2+)离子之间的配位反应在环境条件下从 20 小时大大加速到 8 分钟。基于这一现象,我们使用 TMPyP 和 CCG 的配合物作为光学探针,用于在水介质中快速和选择性检测 Cd(2+)离子。