Zuowei
Xie
a and
Guo-Xin
Jin
b
aDepartment of Chemistry, The Chinese University of Hong Kong, Shatin N.T., Hong Kong, China. E-mail: zxie@cuhk.edu.hk
bDepartment of Chemistry, Fudan University, Shanghai, 200433, China. E-mail: gxjin@fudan.edu.cn
o-Carboranes can be converted into nido-C2B9H112− by selective removal of a BH vertex, nido-C2B10H122− or arachno-C2B10H124−via reduction with group 1 metals. These anions are excellent π ligands for transition metals or serve as useful synthons for the preparation of supraicosahedral carboranes/heterocarboranes through polyhedral expansion methodology. On the other hand, o-carboranes can undergo deprotonation reaction to give either monoanion LiC2B10H11− or dianion Li2C2B10H102−, which react further with electrophiles to generate a class of carborane-based ligands for transition metals. In addition, o-carboranes can also be functionalized via o-carborynes (1,2-dehydro-o-carboranes) intermediates. These functional carboranes are finding applications in materials science as building blocks and in medicine as potent boron neutron capture therapy agents.
The collection of papers presented in this themed issue encompasses all aspects aforementioned across a broad spectrum of carborane derivatives, reflecting the current research interests in this field. We hope that readers will find this timely collective volume interesting and stimulating. We would like to take this opportunity to thank all contributors, reviewers, and the editorial team for their high quality and professional work.
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