A novel tridentate co-ordination mode for the carbonatonickel system
A novel tridentate co-ordination mode for the carbonatonickel system
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DOI:
10.1039/a605466h
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发表时间:
1997-02-07
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影响因子:
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通讯作者:
FontBardia, M
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文献类型:
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作者:
Escuer, A;Vicente, R;FontBardia, M
The trinuclear compound [Ni-2(mu-Co-3)(dmpd)(4)(H2O)][Ni(dmpd)(2)(H2O)(2)][ClO4](4) . H2O was obtained from the reaction of basic solutions of nickel(II) perchlorate and 2,2-dimethylpropane-1,3-diamine (dmpd) with atmospheric CO2 It crystallises in the orthorhombic system, space group Pcab, with a = 18.634(10), b = 25.447(8), c = 25.598(4) Angstrom, Z = 8, R = 0.0437. The three nickel atoms show octahedral co-ordination with three different environments; Ni(CO3-O,O')(dmpd)(2), Ni(CO3-O '')(dmpd)(2)(H2O) and Ni(dmpd)(2)(H2O)(2). The carbonate anion acts as a bridge between two nickel ions whereas the [Ni(dmpd)(2)(H2O)(2)](2+) subunit is linked by hydrogen bonds to the dinuclear group. The dinuclear [Ni-2(mu-CO3)(dmpd)(4)(H2O)](2+) subunit shows a moderately weak antiferromagnetic coupling with a J value of -7.8 cm(-1). The tridentate co-ordination mode found in the carbonate ligand has not previously been reported for nickel. Its magnetic behaviour is discussed.