Source:http://linkedlifedata.com/resource/pubmed/id/18404753
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
15
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pubmed:dateCreated |
2008-5-14
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pubmed:abstractText |
Reaction between the optically active metal-free phthalocyanine with a pi system with noncentrosymmetrical C(2) [corrected] symmetry ((S)- and (R)-H(2){Pc(OBNP)(2)}; OBNP=binaphthylphthalocyanine) and half-sandwich complexes [M(III)(acac)(TClPP)] (M=Y, Eu; TClPP=meso-tetrakis(4-chlorophenyl)porphyrinate; acac=acetylacetonate), which were generated in situ from [M(acac)(3)].n H(2)O and H(2)(TClPP) in n-octanol at reflux, provided the first optically active protonated mixed phthalocyaninato-porphyrinato rare-earth double-decker complexes [M(III)H{Pc(OBNP)(2)}(TClPP)] (M=Y, Eu) in good yield. In addition to electronic absorption spectroscopy and magnetic circular dichroism results, circular dichroism shows different spectroscopic features of these mixed-ring rare-earth double-decker compounds in different solvents, such as DMF and CHCl(3), which was well-reproduced on the basis of time-dependent density functional theory calculation results for the yttrium species (S)-[Y(III){Pc(OBNP)(2)}(Por)](-) (Por=porphyrinate, which is obtained by removing the four chlorophenyl groups from the TClPP ligand) in terms of the change in the rotation angle between the two macrocyclic ligands in the double-decker molecules. These results revealed the solvent-dependent nature of the molecular conformation of mixed-ring rare-earth double-decker complexes, which suggests a new way of tuning the optical and the electrochemical properties of sandwich-type bis(tetrapyrrole)-metal double-decker complexes in solution by changing the solvent.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Indoles,
http://linkedlifedata.com/resource/pubmed/chemical/Metalloporphyrins,
http://linkedlifedata.com/resource/pubmed/chemical/Metals, Rare Earth,
http://linkedlifedata.com/resource/pubmed/chemical/Solvents,
http://linkedlifedata.com/resource/pubmed/chemical/phthalocyanine
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pubmed:status |
MEDLINE
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pubmed:issn |
0947-6539
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4667-74
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pubmed:dateRevised |
2009-8-4
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pubmed:meshHeading |
pubmed-meshheading:18404753-Circular Dichroism,
pubmed-meshheading:18404753-Indoles,
pubmed-meshheading:18404753-Metalloporphyrins,
pubmed-meshheading:18404753-Metals, Rare Earth,
pubmed-meshheading:18404753-Models, Molecular,
pubmed-meshheading:18404753-Molecular Conformation,
pubmed-meshheading:18404753-Solvents
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pubmed:year |
2008
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pubmed:articleTitle |
Optically active mixed phthalocyaninato-porphyrinato rare-earth double-decker complexes: synthesis, spectroscopy, and solvent-dependent molecular conformations.
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pubmed:affiliation |
Key Lab for Colloid and Interface Chemistry of Education Ministry, Department of Chemistry, Shandong University, Jinan, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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