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11.
Rahul Bhattacharya Sumana Chanda Andrea Cantoni Gabriele Bocelli Ashutosh Ghosh 《Journal of chemical crystallography》2004,34(5):325-331
The crystal structures of benzimidazolium tetrahalocobaltates (HBz)2[CoX4] (X = Cl and Br) have been determined. The chloride salt is triclinic, P-1, with a = 7.670(3) Å, b = 8.307(3) Å, c = 15.730(2) Å, and = 87.37(3)°, = 84.99(3)°, = 67.72(2)°. The bromide salt is monoclinic, C2/c, with a = 15.568(2) Å, b = 8.063(3) Å, c = 5.762(2) Å and = 91.36(3)°. The structures of the two salts are closely related. Both the compounds contain isolated tetrahedral CoX4
2– anions and benzimidazolium cations. In the chloride salt, three chloride ions are involved in strong hydrogen bonding while only two bromide ions participate in the bromide salt. The greater deviation from the ideal tetrahedral geometry in CoBr4
2– can be related to the less extensive hydrogen-bonding network compared to the chloro complex. 相似文献
12.
The reaction of bisbenzimidazolium salt with Grignard reagents and a new synthetic method of a‐diketones from bis‐benzimidazolium salt and Grignard reagents are reported. The structures of all a‐diketones are characterized by elemental analyses, infrared spectroscopy and 1H NMR spectroscopy. The influences of the various Grignard reagents on the yield of a‐diketones and the mechanism are discussed, and a new convenient synthetic method for a‐diketones is provided. 相似文献
13.
《应用有机金属化学》2017,31(8)
A series of ionic iron(III) complexes of general formula [HLn ][FeX4] (HL1 = 1,3‐dibenzylbenzimidazolium cation, X = Cl, 1 ; HL1, X = Br, 2 ; HL2 = 1,3‐dibutylbenzimidazolium cation, X = Br, 3 ; HL3 = 1,3‐bis(diphenylmethyl)benzimidazolium cation, X = Br, 4 ) were easily prepared in high yields by the direct reaction of FeX3 with 1 equiv. of [HLn ]X under mild conditions. All of them were characterized using elemental analysis, Raman spectroscopy and electrospray ionization mass spectrometry, and X‐ray crystallography for 1 and 4 . In the presence of magnesium turnings and LiCl, these air‐ and moisture‐insensitive complexes showed high catalytic activities in direct cross‐couplings of aryl phosphates with primary and secondary alkyl bromides with broad substrate scope, wherein complex 4 was the most effective. 相似文献
14.
Sunusi Y. Hussaini Rosenani A. Haque Jing‐Hong Li Shun‐Ze Zhan Kong Wai Tan Mohd. R. Razali 《应用有机金属化学》2019,33(6)
A new series of N‐heterocyclic carbene (NHC) ligand precursors ( 1 and 2 ) with their [Ag(I)(NHC)2]PF6 complexes ( 3 and 4 ) and [ClAu(I)(NHC)] complexes ( 5 and 6 ) are reported. Complexes 5 and 6 were synthesized via transmetalation reaction using either 3 or 4 and AuCl(SMe2) as reactants, respectively. All the synthesized compounds were fully characterized using elemental analyses and Fourier transform infrared, 1H NMR and 13C NMR spectroscopies. In the crystal structures of 3 , 5 and 6 , the Ag(I) and Au(I) ions are in a linear geometry. The entire structure of 3 is stabilized by significant π–π interactions, while the structures of 5 and 6 are stabilized with the presence of aurophilic interactions between the adjacent Au(I) ions as well as CH–π or π–π interactions. From photoluminescence studies, complexes 5 and 6 show dual‐emission characteristics. The higher‐energy fluorescence originates from 1XLCT mixed with 1MLCT, while the lower‐energy phosphorescence is ascribed to 3XLCT and 3MLCT with small contribution of 3ILCT, as evidenced by density functional theory (DFT) and time‐dependent DFT calculations of the modelled molecules. 相似文献
15.
Rafet Kılınçarslan M. Emin Günay Rukiye Fırıncı Serpil Denizaltı Bekir Çetinkaya 《应用有机金属化学》2016,30(5):268-272
A new series of sterically hindered ligands containing (1R,2S,4R)‐(+)‐menthoxymethyl group attached to benzimidazole‐based N‐heterocyclic carbene (NHC), palladium–bis‐NHC complexes and (κ2‐C,N)‐palladacyclic NHC complexes have been synthesized and characterized using appropriate spectroscopic techniques. Catalytic performance of the palladium complexes has been investigated for allylic alkylation, Suzuki and Heck carbon–carbon coupling reactions. These complexes smoothly catalyse the carbon–carbon bond formation reactions. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
16.
Kumaresh Ghosh Debasis Kar Atanu Panja Ioannis D. Petsalakis Giannoula Theodorakopoulos 《Supramolecular chemistry》2013,25(10-12):856-863
A series of pyridine-coupled benzimidazolium-based receptors 1, 2 and 3 have been designed and synthesised. In the series, only receptor 1 is structurally appealing in the selective recognition of H2PO4? in CHCl3 as well as in CH3CN over a series of other anions. The ratiometric change in emission with a triplet band at 420 nm is the distinctive feature of selective recognition of H2PO4? in CHCl3. In CH3CN, a ‘turn on’ response is selectively observed. Binding studies have been carried out using fluorescence, UV–vis, 1H NMR and 31P NMR spectroscopic techniques. Experimental results have been correlated with the theoretical findings. 相似文献
17.
SHI Zhen WANG Luyao GU Huan LI Jianli BAI Yinjuan & YANG Bingqin Department of Chemistry Northwest University Xi''''an China 《中国科学B辑(英文版)》2005,48(Z1)
A facile and efficient method for the formylation of Grignard reagent was reported, and a new approach for the preparation of aldehydes from Grignard reagent and benzimida-zolium salts was provided. 相似文献
18.
19.
A new synthetic method of ketones from substituted benzimidazolium salts and Grignard reagents is reported. The influences of the various Grignard reagents on the yield of ketones and the mechanism are discussed. 相似文献
20.
A new approach to the synthesis of α,β-unsaturated ketones from 1,2,3-trimethyl benzimidazolium salt via the condensation reaction with aldehydes followed by the addition reaction of Grignard reagents with quaternary C=N bond was provided. 相似文献