Title of article :
The Remarkable Reactivity of High Oxidation State Ruthenium and Osmium Polypyridyl Complexes
Author/Authors :
Meyer، Thomas J. نويسنده , , Huynh، My Hang V. نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2003
Pages :
-813
From page :
814
To page :
0
Abstract :
The tripodal ligand 1,3,5-(CH3)3C6[CH2OCH2C(pz)3]3 (L1, pz = pyrazolyl ring) reacts with AgBF4 to yield {[L12Ag3(CH3CN)]. (BF4)3}.(CH3CN)4, an inclusion complex in which the encapsulated acetonitrile cannot escape the triangular cage unit in either the solid or solution phase. The analogous hexatopic ligand C6[CH2OCH2C(pz)3]6 forms a 2-dimensional polymer composed of similar triangular cage units, again with the encapsulation of one acetonitrile molecule, linked by the additional tris(pyrazolyl)methane units. In contrast, the complex formed with L1 and Cd2+ has a double, open cage structure holding two diethyl ether molecules.
Keywords :
dynamic , Chiral , Computations , Triphenylphosphines
Journal title :
INORGANIC CHEMISTRY
Serial Year :
2003
Journal title :
INORGANIC CHEMISTRY
Record number :
66530
Link To Document :
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