Source:http://linkedlifedata.com/resource/pubmed/id/12716168
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
9
|
| pubmed:dateCreated |
2003-4-28
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| pubmed:abstractText |
A new class of sterically hindered phthalocyanine has been synthesized and characterized. Pentaphenylbenzene units were introduced at the periphery of each phthalocyanine to yield a sterically protected metal center. The attachment of the bulky oligophenylbenzene units resulted in the complete isolation of individual MPc molecules. The pockets around a cobalt center affect selectivity in the ligation of pyridines that have different sizes and shapes.
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| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:status |
PubMed-not-MEDLINE
|
| pubmed:month |
May
|
| pubmed:issn |
0020-1669
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| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
5
|
| pubmed:volume |
42
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
2821-3
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| pubmed:year |
2003
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| pubmed:articleTitle |
Selective ligation to sterically isolated metallophthalocyanines.
|
| pubmed:affiliation |
Department of Functional Polymer Science, Faculty of Textile Science and Technology, Shinshu University, Ueda 386-8567, Japan. mkimura@giptc.shinshu-u.ac.jp
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| pubmed:publicationType |
Journal Article
|