http://www.cnr.it/ontology/cnr/individuo/prodotto/ID271538
Synthesis and photo-physical properties of a series of BODIPY dyes (Articolo in rivista)
- Type
- Label
- Synthesis and photo-physical properties of a series of BODIPY dyes (Articolo in rivista) (literal)
- Anno
- 2013-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.tet.2013.04.064 (literal)
- Alternative label
Banfi, Stefano; Nasini, Gianluca; Zaza, Stefano; Caruso, Enrico (2013)
Synthesis and photo-physical properties of a series of BODIPY dyes
in Tetrahedron (Oxf., Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Banfi, Stefano; Nasini, Gianluca; Zaza, Stefano; Caruso, Enrico (literal)
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- Note
- ISI Web of Science (WoS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- University of Insubria; Polytechnic University of Milan; Shimadzu Italia Srl (literal)
- Titolo
- Synthesis and photo-physical properties of a series of BODIPY dyes (literal)
- Abstract
- A series of 39 boron-dipyrrolylmethenes (BODIPYs) have been synthesized and characterized. Their spectroscopic properties, degree of lipophilicity, chemical stability under irradiation, and singlet-oxygen generation rate have also been studied. These compounds differ in the presence of ethyl groups (group A), hydrogens (group B) or iodines (group C) on the 2,6 positions; these appendices confer particular characteristics to each group. The presence of an aromatic substituent or hydrogen on the indacene 8 position produces 13 different molecules of each group. Besides the effects exerted by the group or atom on the 2,6 positions, the substituent on the 8 position exerts a further effect on the physico-chemical parameters, thus the desired properties of BODIPYs, concerning fluorescence, lipophilicity, and singlet oxygen production can be modulated accordingly. (C) 2013 Elsevier Ltd. All rights reserved. (literal)
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