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Regioselective Exohedral Functionalization of La@C82 and its 1,2,3,4,5‐Pentamethylcyclopentadiene and Adamantylidene Adducts
Authors:Yutaka Maeda Prof Dr  Satoru Sato  Koji Inada  Hidefumi Nikawa  Michio Yamada Dr  Naomi Mizorogi Dr  Tadashi Hasegawa Prof Dr  Takahiro Tsuchiya Dr  Takeshi Akasaka Prof Dr  Tatsuhisa Kato Prof Dr  Zdenek Slanina Dr  Shigeru Nagase Prof Dr
Institution:1. Department of Chemistry, Tokyo Gakugei University, Koganei, Tokyo 184‐8501 (Japan), Fax: (+81)?42‐329‐7496;2. Center for Tsukuba Advanced Research Alliance, University of Tsukuba, Tsukuba 305‐8577 (Japan), Fax: (+81)?29‐853‐6409;3. Department of Chemistry, Josai University, Sakado, Saitama 171‐8501 (Japan);4. Department of Theoretical and Computational Molecular Science, Institute for Molecular Science, Myodaiji, Okazaki 444‐8585 (Japan), Fax: (+81)?564‐53‐4660
Abstract:The first regioselective functionalization of La@C82 by two different groups has been performed. Bis‐adducts of La@C82 with Cp* and adamantylidene were synthesized by using two different routes and characterized. Spectroscopic analysis and theoretical calculations reveal that the addition position is controlled by the charge density and p‐orbital axis vector value of the fullerene cage.
Keywords:carbenes  cycloaddition  fullerenes  lanthanum  regioselectivity
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