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Unexpected behaviour of copper(I) towards a tridentate Schiff base: synthesis, structure and properties of new Cu(I)Cu(II) and Cu(II) complexes
The reaction of CuBr with 2,6-bis[1-(2,6-diisopropylphenylimino)ethyl]pyridine L afforded a new Cu(I)Cu(II) derivative [CuBrL] 2[Cu 2Br 4] ( 1), while the reaction of [Cu(CH 3CN) 4]PF 6 with L in THF yielded the new Cu(I) compound CuL(THF)(CH 3CN)PF 6 ( 2). Derivative 2 further reacted with halogen...
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Published in: | Inorganica Chimica Acta 2001-11, Vol.324 (1), p.300-308 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The reaction of CuBr with 2,6-bis[1-(2,6-diisopropylphenylimino)ethyl]pyridine L afforded a new Cu(I)Cu(II) derivative [CuBrL]
2[Cu
2Br
4] (
1), while the reaction of [Cu(CH
3CN)
4]PF
6 with L in THF yielded the new Cu(I) compound CuL(THF)(CH
3CN)PF
6 (
2). Derivative
2 further reacted with halogenated solvents to yield halogeno-Cu(II) salts, [CuClL]PF
6 (
3) using CHCl
3 and [CuBrL]Br
3 (
4) using CHBr
3. Compounds
1,
3 and
4 have been fully characterised by X-ray crystallography; they contain essentially similar [CuXL]
+ cations with a square planar copper(II) co-ordination. However, the structure of compound
1 must be viewed as built of tetranuclear units since two [Cu
IIBrL]
+ cations are bridged by a [Cu
I
2Br
4]
2− anion with a rather strong Cu
II⋯Br (2.689(2) Å) secondary interaction. These secondary interactions (Cu
II cation⋯FPF
5 or Br anion) are weaker in
3 and
4. The electrochemical properties of compounds
1–
4 are discussed, too.
The reaction of CuBr with a pyridine/di-imine ligand L afforded a new Cu(I)Cu(II) derivative [CuBrL]
2[Cu
2Br
4] (
1), while the reaction of [Cu(CH
3CN)
4]PF
6 with L in THF yielded the new Cu(I) compound {CuL(THF)(CH
3CN)(PF
6)}(
2). Compound
2 reacts with halogenated solvants to give halogeno-Cu(II) derivatives, [CuClL]PF
6 (
3) [CuBrL]Br
3 (
4). Compounds
1,
3 and
4 have been fully characterised by X-ray crystallography and electrochemistry. |
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ISSN: | 0020-1693 1873-3255 0020-1693 |
DOI: | 10.1016/S0020-1693(01)00663-6 |