Reactions of rhodium and iridium salts with multidentate N-heterocycles

Gayathri, V.; Leelamani, E.G.; Gowda, N. M. Nanje; Reddy, G.K.N.

doi:10.1016/s0277-5387(96)00368-3

Cited by 21 publications

(10 citation statements)

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“…As part of our continuing research in the field of syntheses of nitrogencontaining heterocyclic ligands and their metal complexes with palladium and rhodium, 3 we are reporting here the synthesis and crystal structure of 6-pyridyl-5,6-dihydrobenzo [4,5]…”

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confidence: 99%

Crystal Structure of 6-Pridyl-5,6-dihydrobenzo[4,5]-imidazo[1,2-c]quinazoline

et al. 2004

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The N-heterocycles are of considerable importance in view of their presence in several biological systems. Benzimidazole derivatives and their metal complexes exhibit anti-bacterial, veterinary, anti-helmintic, insecticidal and virucidal activities. 1 Multidentate N-heterocycles produce organized supramolecules on coordination to metal ions and they appear quite promising for the design of stable light conversion devices. 2In this direction, some of the multidentate N-heterocycles and their complexes have been prepared and characterized. As part of our continuing research in the field of syntheses of nitrogencontaining heterocyclic ligands and their metal complexes with palladium and rhodium, 3 we are reporting here the synthesis and crystal structure of 6-pyridyl-5,6-dihydrobenzo [4,5]The synthesised ligand was characterized by physical, spectral and single crystal X-ray structural analyses.o-Aminophenylbenzimidazole (0.05 mol: 10.45 g) was dissolved in 200 ml of alcohol. To this, 2-pyridylinaldehyde (0.05 mol; 4.75 g) was added, and the mixture was refluxed for 4 -5 hours. The chemical structure is as shown in Fig. 1. A yellow compound was obtained. It was concentrated under reduced pressure. The solid was recrystallized from methanol to get a pure compound. A suitable crystal for X-ray analysis was grown by the slow evaporation method using methanol as solvent.A single crystal of the title ligand of dimensions 0.2 × 0.4 × 0.5 mm was chosen for X-ray diffraction studies. The measurements were made on a Rigaku AFC7S diffractometer with graphite-monochromated radiation (Mo Kα). The data were collected using the ω-2θ scan technique and reduced using the teXsan data reduction program. 4 Lorentz and polarization corrections were applied. The structure was solved by direct methods and refined by a full-matrix least squares method with anisotropic temperature factors for the non-H atoms. All the H atoms were placed at chemically acceptable positions and were refined with isotropic temperature factors. The experimental crystallographic details are given in Table 1.The final coordinates and equivalent thermal parameters of non-H atoms are listed in Table 2. Table 3 gives the bond distances and angles of non-hydrogen atoms. The bond distances and bond angles are in good agreement with the standard values. The title compound C19H12N4 was synthesised and the structure was investigated by X-ray crystallography. It crystallizes in the monoclinic space group P21/c with cell parameters a = 8.697(9)Å, b = 13.045(10)Å, c = 13.271(4)Å, β = 97.38(4)å nd Z = 4. The final residual factor is 0.0628.

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confidence: 99%

Crystal Structure of 6-Pridyl-5,6-dihydrobenzo[4,5]-imidazo[1,2-c]quinazoline

et al. 2004

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“…10,[19][20] PdCl 2 was procured from Arora-Matthey Ltd. and 1,5-cyclooctadiene was obtained from Merck. and [PdX(cotl)] 2 (X = Cl or Br) were prepared as described earlier.…”

Section: Methodsmentioning

confidence: 99%

Synthesis and Characterisation of Palladium(II) Complexes with 1,2-bis(N-methylbenzimidazolyl)Benzene

Bheemanna

Gayathri

Gowda

2006

Journal of Chemical Research

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“…Compound 4 shows resonances for C-8Ј and C-9Ј at 133.1, clear indication that protonation occurred [21]. The effect of the lone pair or of the N-H over the nearest ipso carbon atoms can also be observed at the anchored ligand 1 (THF-d 8 ) where C-9Ј appears at 145.1 ppm, C-8Ј at 134.7, C-4Ј at 120, and C-7Ј at 110.9.…”

Section: Protonation Reactionsmentioning

confidence: 97%

“…Herein, we present some of our results in the study of the coordinating behavior of 2,6-bis(benzimi- dazol-2Ј-yl)pyridine (1), which is a useful and frequently used ligand for metal complexation [1][2][3][4][5][6][7][8][9]. This study is part of our continuing interest in the coordinating ability of aromatic nitrogenated molecules bearing sp 2 nitrogen atoms as present in pyrrole, pyridine, imines, anilines, or imidazole, especially because they can be part of strongly basic polydentate ligands [10][11][12][13][14][15][16][17][18][19][20][21][22].…”

Section: Introductionmentioning

confidence: 99%