Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
17
pubmed:dateCreated
2008-8-28
pubmed:abstractText
The treatment of boron(III) subphthalocyanine chloride (SPcCl) with 3- or 4-hydroxypyridine in the presence of pyridine in toluene gave the corresponding boron(III) subphthalocyanine pyridinolates SPc(3-OPy) ( 1) or SPc(4-OPy) ( 2). Having a pyridyl group, these compounds could axially complex with a series of zinc(II) and ruthenium(II) porphyrins and phthalocyanines to form the corresponding subphthalocyanine-porphyrin and subphthalocyanine-phthalocyanine heterodyads. As revealed by UV-vis spectroscopy, the ground-state interaction between the two chromophores in these dyads is insignificant. The complexation processes were also studied by (1)H NMR and fluorescence spectroscopic methods, which confirmed the 1:1 binding stoichiometry. The association constants, as determined by fluorescence titration, were generally higher for the ruthenium(II) tetrapyrroles [(2.5-4.7) x 10 (4) M (-1)] than for the zinc(II) counterparts [(0.3-1.8) x 10 (4) M (-1)]. The molecular structures of the two pyridyl subphthalocyanines 1 and 2, together with three novel subphthalocyanine-porphyrin heterodyads, were also determined by X-ray diffraction analyses.
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Sep
pubmed:issn
1520-510X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
1
pubmed:volume
47
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
7921-7
pubmed:year
2008
pubmed:articleTitle
Construction of subphthalocyanine-porphyrin and subphthalocyanine-phthalocyanine heterodyads through axial coordination.
pubmed:affiliation
Department of Chemistry and Center of Novel Functional Molecules, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China. dkpn@cuhk.edu.hk
pubmed:publicationType
Journal Article