Source:http://linkedlifedata.com/resource/pubmed/id/19053414
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
51
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| pubmed:dateCreated |
2008-12-18
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| pubmed:abstractText |
Improving the nonlinear optical properties of organic materials through transition to macromolecular architectures of highly conjugated chromophores has been shown to be a viable strategy for generating materials suitable for TPA applications. In this study we display a simple and elegant method by which to synthesize macrocycles of porphyrin dimers. Two-photon absorption studies show 2 orders of magnitude enhancement of cross-section of the material, giving a maximum delta(2) of 10(6) GM.
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:status |
PubMed-not-MEDLINE
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| pubmed:month |
Dec
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| pubmed:issn |
1520-5126
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| pubmed:author | |
| pubmed:issnType |
Electronic
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| pubmed:day |
24
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| pubmed:volume |
130
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| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
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| pubmed:pagination |
17212-3
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| pubmed:year |
2008
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| pubmed:articleTitle |
Synthesis and two-photon absorption enhancement of porphyrin macrocycles.
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| pubmed:affiliation |
Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, USA.
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| pubmed:publicationType |
Journal Article
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