<?xml version="1.0" encoding="UTF-8"?>
<collection>
<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1021/acs.inorgchem.6b02826</dc:identifier><dc:language>eng</dc:language><dc:creator>Fuertes, S.</dc:creator><dc:creator>Chueca, A.J.</dc:creator><dc:creator>Arnal, L.</dc:creator><dc:creator>Martín, A.</dc:creator><dc:creator>Giovanella, U.</dc:creator><dc:creator>Botta, C.</dc:creator><dc:creator>Sicilia, V.</dc:creator><dc:title>Heteroleptic Cycloplatinated N-Heterocyclic Carbene Complexes: A New Approach to Highly Efficient Blue-Light Emitters</dc:title><dc:identifier>ART-2017-99044</dc:identifier><dc:description>New heteroleptic compounds of platinum(II)-containing cyclometalated N-heterocyclic carbenes, [PtCl(R-C^C*)(PPh3)] [R-CH^C*-?C* = 3-methyl-1-(naphthalen-2-yl)-1H-imidazol-2-ylidene (R-C = Naph; 1A), 1-[4-(ethoxycarbonyl)phenyl]-3-methyl-1H-imidazol-2-ylidene (R = CO2Et; 1B), and [Pt(R-C^C*)(py)(PPh3)]PF6 (py = pyridine; R-C = Naph, 2A; R = CO2Et, 2B], have been prepared and fully characterized. All of them were obtained as the trans-(C*, PPh3) isomer in high yields. The selectivity of their synthesis has been explained in terms of the degree of transphobia (T) of pairs of ligands in trans positions. X-ray diffraction studies on both 2A and 2B revealed that only in 2A, containing a C^C* with a more extended p system, do the molecules assemble themselves into head-to-tail pairs through intermolecular p···p contacts. The photophysical properties of 2A and 2B and those of the related compounds [Pt(NC-C^C*)(PPh3)L]PF6 [NC-CH^C*-?C* = 1-(4-cyanophenyl)-3-methyl-1H-imidazol-2-ylidene; L = pyridine (py; 2C), 2, 6-dimethylphenylisocyanide (CNXyl; 3C), and 2-mercapto-1-methylimidazole (MMI; 4C)] have been examined to analyze the influence of the R substituent on R-C^C* (R-C = Naph; R = CO2Et, CN) and that of the ancillary ligands (L) on them. Experimental data and time-dependent density functional theory calculations showed the similarity of the electronic features associated with R-C^C* (R = CN, CO2Et) and their difference with respect to R-C^C* (R-C = Naph). All of the compounds are very efficient blue emitters in poly(methyl methacrylate) films under an argon atmosphere, with QY values ranging from 68% (2B) to 93% (2C). In the solid state, the color of the emission changes to yellowish-orange for compounds 2A (?max = 600 nm) and 3C (?max = 590 nm) because of the formation of aggregates through intermolecular p···p interactions. 2C and 3C were chosen to fabricate fully solution-processed electroluminescent devices with blue-light (2C), yellow-orange-light (3C), and white-light (mixtures of 2C and 3C) emission from neat films of the compounds as emitting layers.</dc:description><dc:date>2017</dc:date><dc:source>http://zaguan.unizar.es/record/69639</dc:source><dc:doi>10.1021/acs.inorgchem.6b02826</dc:doi><dc:identifier>http://zaguan.unizar.es/record/69639</dc:identifier><dc:identifier>oai:zaguan.unizar.es:69639</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E21</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/CTQ2015-67461-P</dc:relation><dc:identifier.citation>Inorganic Chemistry 56, 9 (2017), 4829-4839</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

</collection>