Surface-Mediated Two-Dimensional Growth of the Pharmaceutical Carbamazepine

被引:18
|
作者
Iski, Erin V. [1 ]
Johnston, Blair F. [2 ]
Florence, Alastair J. [2 ]
Urquhart, Andrew J. [2 ]
Sykes, E. Charles H. [1 ]
机构
[1] Tufts Univ, Dept Chem, Pearson Chem Lab, Medford, MA 02155 USA
[2] Univ Strathclyde, Strathclyde Inst Pharm & Biomed Sci, Glasgow G4 0NR, Lanark, Scotland
基金
美国国家科学基金会; 英国工程与自然科学研究理事会;
关键词
carbamazepine; polymorph; heteronuclei; surface; STM; SCANNING-TUNNELING-MICROSCOPY; CAMBRIDGE STRUCTURAL DATABASE; SELF-ASSEMBLED MONOLAYERS; CRYSTAL-STRUCTURES; ORGANIC-MOLECULES; ULTRAHIGH-VACUUM; CHIRALITY; STM; NETWORK; ORGANIZATION;
D O I
10.1021/nn100868r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Scanning tunneling microscopy (STM) has become a staple surface microscopy technique for a number of research fields ranging from semiconductor research to heterogeneous catalysis. Pharmaceutical compounds, however, remain largely unstudied. Here we report the first STM study of carbamazepine (CBZ), an anti-epileptic drug, on Au(111) and Cu(111) surfaces. The analysis reveals that CBZ adopts unusual chiral molecular architectures on both metals. These previously unreported structures, which are strikingly different from CBZ packing arrangements observed in 3D crystal structures, indicate that the main molecular architecture is driven by a combination of CBZ intermolecular hydrogen bonding and metal-CBZ interactions. Comparison of the 2D molecular structures reveals large differences in local geometry and packing density that are dependent on the nature of the metal surface. These results have implications for the potential role of metal surfaces as heteronuclei or templating agents for controlling polymorph formation, which continues to be a problem for many compounds in the pharmaceutical industry including CBZ.
引用
收藏
页码:5061 / 5068
页数:8
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