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<dc:title>Highly fluorescent complexes with 3-isocyanoperylene and N-(2,5-di-tert-butylphenyl)-9-isocyano-perylene- 3,4-dicarboximide</dc:title>
<dc:creator>Lentijo, S.</dc:creator>
<dc:creator>Exposito Fuertes, José Emilio</dc:creator>
<dc:creator>Aullón, Gabriel</dc:creator>
<dc:creator>Miguel García, Jesús Ángel</dc:creator>
<dc:creator>Espinet Rubio, Pablo</dc:creator>
<dc:subject>Chemistry</dc:subject>
<dc:description>Producción Científica</dc:description>
<dc:description>The perylene derivatives 3-isocyanoperylene (Per–N≡C) (4a) and N-(2,5-di-tert-butylphenyl)-&#xd;
9-isocyano-perylene-3,4-dicarboximide (PMI–N≡C) (4b) were prepared and used to synthesize&#xd;
gold complexes [AuX(CNR)] (X = C6F5 (5a,b), C6F4-OnBu-p (6b)). The reaction of 5b and 6b&#xd;
with HNEt2 led the carbene complexes [AuX{C(NEt2)(NHR)}] (7b, 8b), respectively. The&#xd;
molecular structure of complexes 7b, 8b have been determined by X-ray diffraction analysis&#xd;
showing intermolecular π–stacking of the perylene groups and C6F5 rings, and no Au···Au&#xd;
interactions. The derivative compounds [M(CO)5(CNR)] (M = Cr (9a,b), Mo (10a,b) or W&#xd;
(11a,b)) and trans-[Pd(CNR)2(C6F3Cl2)2] (12a,b) were also prepared. All complexes exhibit&#xd;
fluorescence associated to the perylene fragment with emission quantum yields, in solution at&#xd;
room temperature, in the range 0.05 – 0.93 and emission lifetimes ~ 4 ns. DFT calculations&#xd;
were performed of the absorption spectra of the ligands Per–N≡C and PMI–N≡C, and&#xd;
representative complexes [Au(C6F5)(CNR)], [Cr(CO)5(CNR)], showing a perylene-dominated&#xd;
intraligand π–π*emissive state, from the HOMO and LUMO orbitals of the perylene&#xd;
chromophore, but with significantly different absorption maxima by influence of the metal&#xd;
fragment, particularly significant in the Per–N≡C derivatives.</dc:description>
<dc:date>2016-12-15T11:55:26Z</dc:date>
<dc:date>2016-12-15T11:55:26Z</dc:date>
<dc:date>2014</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>Dalton Transactions, 2014, 43, p. 10885-10897</dc:identifier>
<dc:identifier>1477-9226</dc:identifier>
<dc:identifier>http://uvadoc.uva.es/handle/10324/21767</dc:identifier>
<dc:identifier>10.1039/C4DT01016G</dc:identifier>
<dc:identifier>Dalton Transactions</dc:identifier>
<dc:language>eng</dc:language>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
<dc:publisher>Royal Society of Chemistry</dc:publisher>
<dc:peerreviewed>SI</dc:peerreviewed>
</ow:Publication>
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