Dataset Information

Structural and Luminescent Properties of Homoleptic Silver(I), Gold(I), and Palladium(II) Complexes with nNHC-tzNHC Heteroditopic Carbene Ligands.

ABSTRACT: Novel silver(I), gold(I), and palladium(II) complexes were synthesized with bidentate heteroditopic carbene ligands that combine an imidazol-2-ylidene (nNHC) with a 1,2,3-triazol-5-ylidene (tzNHC) connected by a propylene bridge. The silver(I) and gold(I) complexes were dinuclear species, [M2(nNHC-tzNHC)2](PF6)2 (M = Ag or Au), with the two bidentate ligands bridging the metal centers, whereas in the palladium(II) complex [Pd(nNHC-tzNHC)2](PF6)2, the two ligands were chelated on the same metal center. Because of the presence of two different carbene units, isomers were observed for the gold(I) and palladium(II) complexes. The molecular structures of the head-to-tail isomer for gold(I) complexes, with a twisted or folded-syn conformation of the bridge between the carbene units, were determined by X-ray diffraction analysis. The study was completed with a systematic structural investigation through density functional theory (DFT) calculations. For palladium(II) species, the head-to-head form was structurally characterized. The dinuclear gold(I) complexes were emissive in the solid state in the blue region (PLQY up to 8%); time-dependent density functional theory (abbreviated as TD-DFT) calculations disclosed that the absorption bands have metal-to-ligand-charge-transfer character and evidenced that the emission occurs from the T1 level (phosphorescence).

SUBMITTER: Monticelli M

PROVIDER: S-EPMC6648577 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

ACCESS DATA

Publications

Structural and Luminescent Properties of Homoleptic Silver(I), Gold(I), and Palladium(II) Complexes with nNHC-tzNHC Heteroditopic Carbene Ligands.

Monticelli Marco M Baron Marco M Tubaro Cristina C Bellemin-Laponnaz Stéphane S Graiff Claudia C Bottaro Gregorio G Armelao Lidia L Orian Laura L

ACS omega 20190226 2

Novel silver(I), gold(I), and palladium(II) complexes were synthesized with bidentate heteroditopic carbene ligands that combine an imidazol-2-ylidene (nNHC) with a 1,2,3-triazol-5-ylidene (tzNHC) connected by a propylene bridge. The silver(I) and gold(I) complexes were dinuclear species, [M2(nNHC-tzNHC)2](PF6)2 (M = Ag or Au), with the two bidentate ligands bridging the metal centers, whereas in the palladium(II) complex [P ...[more]

PMID: 31459629

Similar Datasets

Project description:The photophysical properties of a series of gold(i) [LAu(C[triple bond, length as m-dash]CR)] (L = PCy3 (1a-4a), RNC (5a), NHC (6a)) and gold(iii) complexes [Au(C^N^C)(C[triple bond, length as m-dash]CR)] (1b-4b) bearing heterocyclic arylacetylide ligands with narrow band-gap are compared. The luminescence of both series are derived from an intraligand transition localized on the arylacetylide ligand (ππ*(C[triple bond, length as m-dash]CR)) but 1a-3a displayed prompt fluorescence (τ PF = 2.7-12.0 ns) while 1b-3b showed mainly phosphorescence (τ Ph = 104-205 μs). The experimentally determined intersystem crossing (ISC) rate constants (k ISC) are on the order of 106 to 108 s-1 for the gold(i) series (1a-3a) but 1010 to 1011 s-1 for the gold(iii) analogues (1b-3b). DFT/TDDFT calculations have been performed to help understand the difference in the k ISC between the two series of complexes. Owing to the different oxidation states of the gold ion, the Au(i) complexes have linear coordination geometry while the Au(iii) complexes are square planar. It was found from DFT/TDDFT calculations that due to this difference in coordination geometries, the energy gap between the singlet and triplet excited states (ΔE ST) with effective spin-orbit coupling (SOC) for Au(i) systems is much larger than that for the Au(iii) counterparts, thus resulting in the poor ISC efficiency for the former. Time-resolved spectroscopies revealed a minor contribution (<2.9%) of a long-lived delayed fluorescence (DF) (τ DF = 4.6-12.5 μs) to the total fluorescence in 1a-3a. Attempts have been made to elucidate the mechanism for the origins of the DF: the dependence of the DF intensity with the power of excitation light reveals that triplet-triplet annihilation (TTA) is the most probable mechanism for the DF of 1a while germinate electron-hole pair (GP) recombination accounts for the DF of 2a in 77 K glassy solution (MeOH/EtOH = 4 : 1). Both 4a and 4b contain a BODIPY moiety at the acetylide ligand and display only 1IL(ππ*) fluorescence with negligible phosphorescence being observed. Computational analyses attributed this observation to the lack of low-lying triplet excited states that could have effective SOC with the S1 excited state.

Project description:Different synthetic methods have been developed to prepare eight new redox-active pincer-type ligands, H(X,Y), that have pyrazol-1-yl flanking donors attached to an ortho-position of each ring of a diarylamine anchor and that have different groups, X and Y, at the para-aryl positions. Together with four previously known H(X,Y) ligands, a series of 12 Ni(X,Y)2 complexes were prepared in high yields by a simple one-pot reaction. Six of the 12 derivatives were characterized by single-crystal X-ray diffraction, which showed tetragonally distorted hexacoordinate nickel(II) centers. The nickel(II) complexes exhibit two quasi-reversible one-electron oxidation waves in their cyclic voltammograms, with half-wave potentials that varied over a remarkable 700 mV range with the average of the Hammett ?(p) parameters of the para-aryl X, Y groups. The one- and two-electron oxidized derivatives [Ni(Me,Me)2](BF4)n (n = 1, 2) were prepared synthetically, were characterized by X-band EPR, electronic spectroscopy, and single-crystal X-ray diffraction (for n = 2), and were studied computationally by DFT methods. The dioxidized complex, [Ni(Me,Me)2](BF4)2, is an S = 2 species, with nickel(II) bound to two ligand radicals. The mono-oxidized complex [Ni(Me,Me)2](BF4), prepared by comproportionation, is best described as nickel(II) with one ligand centered radical. Neither the mono- nor the dioxidized derivative shows any substantial electronic coupling between the metal and their bound ligand radicals because of the orthogonal nature of their magnetic orbitals. On the other hand, weak electronic communication occurs between ligands in the mono-oxidized complex as evident from the intervalence charge transfer (IVCT) transition found in the near-IR absorption spectrum. Band shape analysis of the IVCT transition allowed comparisons of the strength of the electronic interaction with that in the related, previously known, Robin-Day class II mixed valence complex, [Ga(Me,Me)2](2+).

Dataset Information

Structural and Luminescent Properties of Homoleptic Silver(I), Gold(I), and Palladium(II) Complexes with nNHC-tzNHC Heteroditopic Carbene Ligands.

Publications

Structural and Luminescent Properties of Homoleptic Silver(I), Gold(I), and Palladium(II) Complexes with <i>n</i>NHC-<i>tz</i>NHC Heteroditopic Carbene Ligands.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure