期刊
CHEMISTRY-AN ASIAN JOURNAL
卷 6, 期 9, 页码 2431-2443出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/asia.201100073
关键词
calixarenes; ionic interactions; phosphine ligands; supramolecular capsules; transition metals
Self-assembly and characterization of heterodimeric diphosphine capsules formed by multiple ionic interactions are described. The first type of capsules is composed of one novel tetrasulfonato-xantphos ligand and one complementary tetraammonium calix[4] arene. Encapsulation of a transition metal is achieved by self-assembly of a rhodium complex containing the tetraanionic diphosphine ligand and a tetracationic calix[4] arene. The second type of capsules is composed of two oppositely charged diphosphine ligands: one tetrasulfonato-xantphos and one tetraammonium-diphosphine (of the xantphos-, DPEphos-, and 1,2-bis(diphenylphosphino) ethane (dppe)type). Bis(metallo) capsules, that is, simultaneous encapsulation of two different transition metals, are created by self-assembly of a palladium or platinum complex containing a tetracationic ligand and a rhodium complex containing a tetraanionic ligand. Diphosphine ligands with different flexibilities and shapes assemble into metallocapsules with a proper capsular structure, as is indicated by H-1 NMR and 1D-NOESY spectroscopy, ESIMS, and modeling studies.
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