2020
DOI: 10.1039/d0dt00214c
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Benzoselenophenylpyridine platinum complexes: green versus red phosphorescence towards hybrid OLEDs

Abstract: The solid solutions of the novel platinum complexes bearing pyridyl benzo[b]selenophenes moieties emitted efficient green and red phosphorescence with absolute quantum yields of 52% (for green) and 11.6% (for red).

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Cited by 19 publications
(7 citation statements)
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“…Selenophene and their derivatives are an important class of heterocyclic systems, studied extensively due to their intrinsic biological activities in addition to their wide applicability in material sciences and technology. [339,340] Interestingly, different methodologies have successfully been reported because of the potential utility of the selenophenes in diverse areas like pharmaceuticals, organic syntheses and materials sciences. [341] Therefore, in quest for the generation of new methods to these vital molecules" Hellwig et al recently developed a transitionmetal-free method for accessing 3,4-bis(butylselanyl)selenophenes 463a-b or 464c-ein moderate to good yields by electrophilic cyclization of 1,3-diynes 461 with dibutyldiselenide 462 using oxone in acetonitrile or alcoholic solvents (Scheme 145).…”
Section: Cleavage Of Se-se/te-te Bonds For the Formation Of Organocha...mentioning
confidence: 99%
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“…Selenophene and their derivatives are an important class of heterocyclic systems, studied extensively due to their intrinsic biological activities in addition to their wide applicability in material sciences and technology. [339,340] Interestingly, different methodologies have successfully been reported because of the potential utility of the selenophenes in diverse areas like pharmaceuticals, organic syntheses and materials sciences. [341] Therefore, in quest for the generation of new methods to these vital molecules" Hellwig et al recently developed a transitionmetal-free method for accessing 3,4-bis(butylselanyl)selenophenes 463a-b or 464c-ein moderate to good yields by electrophilic cyclization of 1,3-diynes 461 with dibutyldiselenide 462 using oxone in acetonitrile or alcoholic solvents (Scheme 145).…”
Section: Cleavage Of Se-se/te-te Bonds For the Formation Of Organocha...mentioning
confidence: 99%
“…Among the uncountable N-heterocyclic systems, pyrazole ring is found in a myriad of vital natural and non-natural products in addition to its presence in some important commercial drugs. [335][336][337][338][339][340] In that context, Perin et al developed a simple and efficient one-pot synthesis of 4-organoselanyl-1H-pyrazoles 485a-j in moderate to excellent yields from α,β-alkynyl hydrazine 483 and diphenyl diselenide 484 with the usage of oxone/EtOH under metal-or halogen-free conditions (Scheme 149). [349] The proposed mechanism for this protocol reported by the authors is displayed in the Scheme 150, in which electrophilic species of selenium 486 are easily generated in-situ by the reaction of diorganyldiselenides 484 with oxone/ethanol in an open-flask at 70 °C.…”
Section: Cleavage Of Se-se/te-te Bonds For the Formation Of Organocha...mentioning
confidence: 99%
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“…Very recently, the first examples of phosphorescent Pt(II) complexes bearing 2- and 3-(2-pyridyl)benzo[ b ]selenophenes 53 and 54 ( Figure 12 ) have been reported [ 89 ]. Though they possess very small differences in the molecular design, these two complexes efficiently emitted green and red phosphorescence with absolute Φ = 0.52 (for green) and 0.11 (for red).…”
Section: Applicationsmentioning
confidence: 99%
“…In this context, selenophenes and their derivatives have been widely studied due to their intrinsic biological activity [22], such as antidepressant [23][24][25][26][27][28], antioxidant [29][30][31][32][33][34][35], anticonvulsant [36,37], antibacterial [38], antitumor [39][40][41][42][43][44][45][46][47], antinociceptive [48], hepatoprotective [49,50] and antiapoptotic agents [51]. Besides, they have also played an important role in the materials science field, being used to build organic light emitting diodes (OLEDs) [52][53][54][55][56][57][58], organic field effect transistors (OFETs) [59][60][61][62][63][64][65][66][67][68]…”
Section: Introductionmentioning
confidence: 99%