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Highly efficient deep-blue emitters based oncisandtransN-Heterocyclic Carbene PtIIAcetylide complexes: Synthesis, photophysical properties, and mechanistic studies


Zhang, Y; Blacque, O; Venkatesan, K (2013). Highly efficient deep-blue emitters based oncisandtransN-Heterocyclic Carbene PtIIAcetylide complexes: Synthesis, photophysical properties, and mechanistic studies. Chemistry - A European Journal, 19(46):15689-15701.

Abstract

We have synthesized cis and trans N-heterocyclic carbene (NHC) platinum(II) complexes bearing σ-alkynyl ancillary ligands, namely [Pt(dbim)2(C[TRIPLE BOND]CR)2] [DBIM=N,N′-didodecylbenzimidazoline-2-ylidene; R=C6H4F (4), C6H5 (5), C6H2(OMe)3 (6), C4H3S (7), and C6H4C[TRIPLE BOND]CC6H5 (8)] and [Pt(ibim)2(C[TRIPLE BOND]CC6H5)2] (9) (ibim=N,N′-diisopropylbenzimidazoline-2-ylidene), starting from [Pt(cod)(C[TRIPLE BOND]CR)2] (COD=cyclooctadiene) and 2 equivalents of [dbimH]Br ([ibimH]Br for complexes 9) in the presence of tBuOK and THF. Mechanistic investigations aimed at uncovering the cis to trans isomerization reaction have been performed on the representative cis complex 5 a [Pt(dbim)2(C[TRIPLE BOND]CC6H5)2] and revealed the isomerization to progress smoothly in good yield when 5 a was treated with catalytic amounts of [Pt(cod)(C[TRIPLE BOND]CR)2] at 75 °C in THF or when 5 a was heated at 200 °C in the solid state under an inert atmosphere. Detailed examination of the reactions points to the possible involvement, in a catalytic fashion, of a solvent-stabilized PtII dialkyne complex in the former case and a Pt0 NHC complex in the latter case, for the transformation of the cis isomer to the corresponding trans complex. Thermal stability and the isomerization process in the solid state have been further investigated on the basis of TGA and DSC measurements. X-ray diffraction studies have been carried out to confirm the solid-state structures of 4 b, 5 a, 5 b, and 9 b. All of the synthesized dialkyne complexes 4–9 exhibit phosphorescence in solution, in the solid state at room temperature (RT), and also in frozen solvent glasses at 77 K. The emission wavelengths and quantum yields have been found to be highly tunable as a function of the alkynyl ligand. In particular, the trans isomer of complex 9 in a spin-coated film (10 wt % in poly(methyl methacrylate), PMMA) exhibits a high phosphorescence quantum yield of 80 %, which is the highest reported for PtII-based deep-blue emitters. Experimental observations and time-dependent density functional theory (TD-DFT) calculations are strongly indicative of the emission being mainly governed by metal-perturbed interligand (3IL) charge transfer.

Abstract

We have synthesized cis and trans N-heterocyclic carbene (NHC) platinum(II) complexes bearing σ-alkynyl ancillary ligands, namely [Pt(dbim)2(C[TRIPLE BOND]CR)2] [DBIM=N,N′-didodecylbenzimidazoline-2-ylidene; R=C6H4F (4), C6H5 (5), C6H2(OMe)3 (6), C4H3S (7), and C6H4C[TRIPLE BOND]CC6H5 (8)] and [Pt(ibim)2(C[TRIPLE BOND]CC6H5)2] (9) (ibim=N,N′-diisopropylbenzimidazoline-2-ylidene), starting from [Pt(cod)(C[TRIPLE BOND]CR)2] (COD=cyclooctadiene) and 2 equivalents of [dbimH]Br ([ibimH]Br for complexes 9) in the presence of tBuOK and THF. Mechanistic investigations aimed at uncovering the cis to trans isomerization reaction have been performed on the representative cis complex 5 a [Pt(dbim)2(C[TRIPLE BOND]CC6H5)2] and revealed the isomerization to progress smoothly in good yield when 5 a was treated with catalytic amounts of [Pt(cod)(C[TRIPLE BOND]CR)2] at 75 °C in THF or when 5 a was heated at 200 °C in the solid state under an inert atmosphere. Detailed examination of the reactions points to the possible involvement, in a catalytic fashion, of a solvent-stabilized PtII dialkyne complex in the former case and a Pt0 NHC complex in the latter case, for the transformation of the cis isomer to the corresponding trans complex. Thermal stability and the isomerization process in the solid state have been further investigated on the basis of TGA and DSC measurements. X-ray diffraction studies have been carried out to confirm the solid-state structures of 4 b, 5 a, 5 b, and 9 b. All of the synthesized dialkyne complexes 4–9 exhibit phosphorescence in solution, in the solid state at room temperature (RT), and also in frozen solvent glasses at 77 K. The emission wavelengths and quantum yields have been found to be highly tunable as a function of the alkynyl ligand. In particular, the trans isomer of complex 9 in a spin-coated film (10 wt % in poly(methyl methacrylate), PMMA) exhibits a high phosphorescence quantum yield of 80 %, which is the highest reported for PtII-based deep-blue emitters. Experimental observations and time-dependent density functional theory (TD-DFT) calculations are strongly indicative of the emission being mainly governed by metal-perturbed interligand (3IL) charge transfer.

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Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:07 Faculty of Science > Department of Chemistry
Dewey Decimal Classification:540 Chemistry
Language:English
Date:2013
Deposited On:07 Feb 2014 15:27
Last Modified:05 Apr 2016 17:30
Publisher:Wiley-VCH Verlag Berlin
ISSN:0947-6539
Publisher DOI:https://doi.org/10.1002/chem.201302196
PubMed ID:24108420

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