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991.
Dr. Yuxuan Hu Dr. Jingsheng Miao Dr. Cheng Zhong Yang Zeng Prof. Shaolong Gong Dr. Xiaosong Cao Xue Zhou Dr. Yu Gu Prof. Chuluo Yang 《Angewandte Chemie (International ed. in English)》2023,62(19):e202302478
Heavy-atom integration into thermally activated delayed fluorescence (TADF) molecule could significantly promote the reverse intersystem crossing (RISC) process. However, simultaneously achieving high efficiency, small roll-off, narrowband emission and good operational lifetime remains a big challenge for the corresponding organic light-emitting diodes (OLEDs). Herein, we report a pure green multi-resonance TADF molecule BN-STO by introducing a peripheral heavy atom selenium onto the parent BN-Cz molecule. The organic light-emitting diode device based on BN-STO exhibited state-of-the-art performance with a maximum external quantum efficiency (EQE) of 40.1 %, power efficiency (PE) of 176.9 lm W−1, well-suppressed efficiency roll-off and pure green gamut. This work reveals a feasible strategy to reach a balance between fast RISC process and narrow full width at half maximum (FWHM) of MR-TADF by heavy atom effect. 相似文献
992.
Solid complexes [REL(NO3)3]n with novel (10,3)-a type three-dimensional networks structure have been assembled using rare earth nitrates and an amide type semirigid tripodal bridging ligand, 1,3,5-tris {[(2′-benzylaminoformyl)phenoxyl]methyl}benzene (L), as building blocks. The complexes were crys- tallized in the orthorhombic system with chiral space group P212121. The whole structure consists of an infinite array of trigonal RE(III) ions bridged by tridentate ligands, and a novel (10,3)-a net is formed, which is very uncommon in the rare earth complexes. At room temperature, the Sm(III), Eu(III), Tb(III), Dy(III) complexes all exhibited characteristic luminescence emissions of central metal ions under UV light excitation. 相似文献
993.
Two new Fischer-type carbene-containing trinuclear transition-metal clusters: (μ
3-S)Co3(CO)7[μ, η
2-SCNEt2] 1 and CoRu2(CO)9[μ
3, η
2-SCNEt2] 2 were obtained by the reaction of tris(N,N-diethyldithiocarbamato)cobalt with Co2(CO)8 and Ru3(CO)12. These clusters contain thiocarboxamido ligand in different coordination modes. The thiocarboxamido ligand served as monometalated
or dimetalated sulfur(diethy1amino) carbene ligand in these clusters. Clusters 1 and 2 were characterized by IR, 1H NMR, and single-crystal X-ray diffraction. 相似文献
994.
Jean d’Angelo Georges Morgant Nour Eddine Ghermani Didier Desmaële Bernard Fraisse François Bonhomme Emma Dichi Mehrez Sghaier Yanling Li Yves Journaux John R.J. Sorenson 《Polyhedron》2008
Purposes of these studies were to synthesize Zn(II) and Co(II) complexes of 3-nitro-4-hydroxybenzoic acid, determine their structures through X-ray crystallography, and obtain their anticonvulsant activities. Thermogravimetric, differential scanning calorimetry, impedance of aqueous solutions and magnetic properties analyses were also determined. Anticonvulsant and related activities of these complexes as well as Zn(II), Co(II), Ni(II) and Mg(II) (5-nitrosalicylato) complexes were determined by the National Institutes of Health, Antiepileptic Development Program. Results of these analyses are presented to document unique bonding features and physical properties of these compounds and their anticonvulsant activities. It is concluded that these compounds have chemical and physical properties that can be used to account for their anticonvulsant activities. 相似文献
995.
The reaction of 4-amino-5-ethyl-2H-1,2,4-triazole-3(4H)-thione (AETT, L1) with 2-thiophen carbaldehyde in methanol leads to the corresponding Schiff-base HL1a. The reaction of L1 with AgNO3 in ethanol gives the ionic complex [{[Ag(L1)]NO3}2]n (1). The ionic complex [(PPh3)2Ag(HL1a)2]NO3 · CH3CN (2) can be obtained by the reaction of HL1a with [(PPh3)2Ag]NO3 in methanol and acetonitrile solution, while its reaction with [(PPh3)2PdCl2] in the presence of sodium acetate in methanol leads to the neutral complex [(PPh3)2Pd(L1a)2] · 4MeOH (3). All the compounds were characterized by infrared spectroscopy, elemental analyses as well as by X-ray diffraction studies. 相似文献
996.
Three ligands with flexible bis-terdentate coordination sites, di(2-pyridylcarbaldehyde)-6,6′-dicarboxylic acid hydrazone-2,2′-bipyridine (H2L1), di(2-acetylpyridyl)-6,6′-dicarboxylic acid hydrazone-2,2′-bipyridine (H2L2) and di(2-pyridylketone)-6,6′-dicarboxylic acid hydrazone-2,2′-bipyridine (H2L3) have been easily prepared. Dinuclear double-stranded helicates Co2(L1)2(ClO4)2(C2H5OH)2(H2O)2 (1), Co2(HL2)(L2)(ClO4)3(C2H5OH)2(H2O)2 (2) and Co2(HL3)(L3)(ClO4)3(H2O)4 (3) based on the ligands, H2L1–3, respectively, have been obtained via self-assembly, their structures were determined by FT-IR, Elemental Analysis, ESI-MS and X-ray diffraction method. 相似文献
997.
Angad Kumar Singh Sanyucta Kumari K. Ravi Kumar B. Sridhar T.R. Rao 《Polyhedron》2008,27(7):1937-1941
998.
Scheuermann S Kretz T Vitze H Bats JW Bolte M Lerner HW Wagner M 《Chemistry (Weinheim an der Bergstrasse, Germany)》2008,14(8):2590-2601
The synthesis, structural characterisation and coordination behaviour of mono- and ditopic p-hydroquinone-based bis(pyrazol-1-yl)methane ligands is described (i.e., 2-(pz2CH)C6H3(OH)2 (2a), 2-(pz2CH)-6-(tBu)C6H2(OH)2 (2b), 2-(pz2CH)-6-(tBu)C6H2(OSiiPr3)(OH) (2c), 2,5-(pz2CH)2C6H2(OH)2 (4)). Ligands 2a, 2b and 4 can be oxidised to their p-benzoquinone state on a preparative scale (2a ox, 2b ox, 4 ox). An octahedral Ni II complex [trans-Ni(2c)2] and square-planar Pd II complexes [Pd2bCl2] and [Pd2b ox Cl2] have been prepared. In the two Pd II species, the ligands are coordinated only through their pyrazolyl rings. The fact that [Pd2bC12] and [Pd2b oxC12] are isolable compounds proves that redox transitions involving the p-quinone substituent are fully reversible. In [Pd2b oxCl2], the methine proton is highly acidic and can be abstracted with bases as weak as NEt(3). The resulting anion dimerises to give a dinuclear macrocyclic Pd II complex, which has been structurally characterised. The methylated ligand 2-(pz2CMe)C6H3O2 (11 ox) and its Pd II complex [Pd11 oxCl2] are base-stable. A new class of redox-active ligands is now available with the potential for applications both in catalysis and in materials science. 相似文献
999.
Himeda Y Onozawa-Komatsuzaki N Miyazawa S Sugihara H Hirose T Kasuga K 《Chemistry (Weinheim an der Bergstrasse, Germany)》2008,14(35):11076-11081
Transfer hydrogenation catalyzed by an iridium catalyst with 4,4'-dihydroxy-2,2'-bipyridine (DHBP) in an aqueous formate solution exhibits highly pH-dependent catalytic activity and chemoselectivity. The substantial change in the activity is due to the electronic effect based on the acid-base equilibrium of the phenolic hydroxyl group of DHBP. Under basic conditions, high turnover frequency values of the DHBP complex, which can be more than 1000 times the value of the unsubstituted analogue, are obtained (up to 81 000 h(-1) at 80 degrees C). In addition, the DHBP catalyst exhibits pH-dependent chemoselectivity for alpha,beta-unsaturated carbonyl compounds. Selective reduction of the C=C bond of enone with high activity are observed under basic conditions. The ketone moieties can be reduced with satisfactory activity under acidic conditions. In particular, pH-selective chemoselectivity of the C=O versus C=C bond reduction was observed in the transfer hydrogenation of cinnamaldehyde. 相似文献
1000.
Anderson DR O'Leary DJ Grubbs RH 《Chemistry (Weinheim an der Bergstrasse, Germany)》2008,14(25):7536-7544
The development of a model system to study ruthenium-olefin complexes relevant to the mechanism of olefin metathesis has been reported recently. Upon addition of the ligand precursor 1,2-divinylbenzene to [RuCl(2)(Py)(2)(H(2)IMes)(==CHPh)] (H(2)IMes=1,3-dimesityl-4,5-dihydroimidazol-2-ylidene), two ruthenium-olefin adducts are formed. Based on (1)H NMR spectroscopy experiments and X-ray crystallographic analysis, these complexes are assigned as side-bound isomers in which the olefin and H(2)IMes ligands are coordinated cis to each other. Herein is reported an investigation of the generality of these observations through variation of the N-heterocyclic carbene ligand and the ligand precursor. 相似文献