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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
25
pubmed:dateCreated
2006-12-4
pubmed:abstractText
Heteroheptanuclear ReM6 (M = Cu 2, Ag 3) complexes of 5,5-diethynyl-2,2'-bipyridine were prepared by the reaction of [M2(mu-dppm)2(MeCN)2]2+ (dppm = bis(diphenylphosphino)methane) with the precursor compound Re(Me3SiC[triple bond]CbpyC[triple bond]CSiMe3)(CO)3Cl in the presence of potassium fluoride by fluoride-catalyzed desilylation. When [Cu2(mu-dppm)2(MeCN)2]2+ reacts directly with Me3SiC[triple bond]CbpyC[triple bond]CSiMe3, a binuclear CuI complex [Cu2(mu-dppm)2(SiMe3C[triple bond]CbpyC[triple bond]CSiMe3)2]2+ (4) was isolated. Further addition of [Cu2(mu-dppm)2(MeCN)2]2+ into a THF-MeOH (3:1, v/v) solution of 4 in the presence of potassium fluoride induced isolation of a tetradecanuclear CuI14 complex [Cu14(mu-dppm)14(C[triple bond]CbpyC[triple bond]C)2]10+, which is composed of a binuclear Cu2(mu-dppm)2 and four triangular trinuclear Cu3 units. Both heteroheptanuclear ReIMI6 and tetradecanuclear CuI14 complexes display luminescence in both solid states and dichloromethane solutions at room temperature with emissive lifetimes in the range of microseconds. The dual emissive feature for the ReM6 and CuI14 complexes is ascribed tentatively to originate from both MLCT [d(Re/Cu) -->pi* (bpy)] and LMCT (acetylide --> M3) transitions. .
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Dec
pubmed:issn
0020-1669
pubmed:author
pubmed:issnType
Print
pubmed:day
11
pubmed:volume
45
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
10371-7
pubmed:year
2006
pubmed:articleTitle
Luminescent hepta- and tetradecanuclear complexes of 5,5'-diethynyl-2,2'-bipyridine capped with triangular trinuclear Cu3/Ag3 cluster units.
pubmed:affiliation
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, the Chinese Academy of Sciences, Fuzhou, Fujian 350002, China.
pubmed:publicationType
Journal Article