scholarly journals Some New Derivatives of Organozirconium(IV) with Pyridinedicarboxylic Acids

2012 ◽  
Vol 9 (2) ◽  
pp. 744-748
Author(s):  
Satish C. Dixit ◽  
Rohit K. Singh

Reactions of dichlorobis(cyclopentadienyl)zirconium(IV) with pyridinedicarboxylic acidsviz. quinolinic acids (QAH2), 2,4-pyridine dicarboxylic acid (PAH2), isocinchomeronic acid (IAH2), cinchomeronic acid (CAH2) and dinicotinic acid (DAH2) were carried out in different stoichiometric ratios. Complexes of the type Cp2Zr(QAH)Cl, Cp2Zr(QAH)2, Cp2Zr(PAH)Cl, Cp2Zr(PAH)2, Cp2Zr(IAH)Cl, Cp2Zr(IAH)2, Cp2Zr(CAH)Cl, Cp2Zr(CAH)2, Cp2Zr(DAH)Cl and Cp2Zr(DAH)2were obtained. These new complexes were characterized on the basis of their elemental analyses, electrical conductance, magnetic moment and spectral data.

2012 ◽  
Vol 9 (1) ◽  
pp. 277-281
Author(s):  
Satish C. Dixit ◽  
Rohit K. Singh

Reactions of dichlorobis(cyclopentadienyl)titanium(IV) with pyridine dicarboxylic acidsviz. quinolinic acid (QAH2), 2,4-pyridine dicarboxylic acid (PAH2), isocinchomeronic acid (IAH2), cinchomeronic acid (CAH2) and dinicotinic acid (DAH2) were carried out in different stoichiometric ratios. Complexes of the type Cp2Ti(QAH)Cl, Cp2Ti(QAH)2, Cp2Ti(PAH)Cl, Cp2Ti(PAH)2, Cp2Ti(IAH)Cl, Cp2Ti(IAH)2, Cp2Ti(CAH)Cl, Cp2Ti(CAH)2, Cp2Ti(DAH)Cl and Cp2Ti(DAH)2were obtained. These new complexes were characterized on the basis of their elemental analyses, electrical conductance, magnetic moment and spectral data.


2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
A. K. Yadava ◽  
H. S. Yadav ◽  
Sanjay Singh ◽  
U. S. Yadav ◽  
D. P. Rao

A series of oxovanadium(IV) complexes of the type [VO(mac)]SO4(where mac = tetraazamacrocyclic ligands derived from condensation of 4,4,4-trifluro-1-(2-furyl)-1,3-butanedione or 4,4,4-trifluro-1-(2-thenyl)-1,3-butanedione withp-phenylenediamine and their reaction withβ-diketones) have been prepared using oxometal ion of vanadium as kinetic template. These complexes have been ascertained by electrical conductance, magnetic moment, elemental analyses, infrared, e.s.r. and electronic spectral data. All the oxovanadium(IV) complexes are five-coordinate ones.


2006 ◽  
Vol 71 (8-9) ◽  
pp. 917-928 ◽  
Author(s):  
V.K. Sharma ◽  
Ankita Srivastava ◽  
Shipra Srivastava

A series of octahedral Ru(III), Rh(III) and Ir(III) complexes have been prepared with tetradentate Schiff bases derived by condensing isatin with 1,2-diaminoethane, 1,3-diaminopropane, 1,4-diaminobutane, 1,2-diaminobenzene and 1,3-diaminobenzene. The obtained complexes were characterized on the basis of their elemental analyses, magnetic moment, conductance, IR electronic, 1HNMR and FAB mass spectra, as well as thermal analyses. The Ru(III) complexes are low spin paramagnetic, while Rh(III) and Ir(III) behave as diamagnetic complexes. The IR spectral data revealed that all the Schiff bases behave as tetradentate and are coordinated to Ru(III), Rh(III) and Ir(III) via nitrogen and oxygen. Antifungal studies of the ligands as well as their complexes were carried out by the agar plate method.


1971 ◽  
Vol 24 (2) ◽  
pp. 405 ◽  
Author(s):  
JL Huppatz ◽  
RMJ Moore

2-Aminothiophenol reacted with β-propiolactone in ethanol to give β-[o- (β-carboxyethylamino)phenylthio]propionic acid (1) which underwent cyclodehydration in polyphosphoric acid to give derivatives of two new heterocyclic ring systems, viz., 1,8-dioxo-1,2,3,4,5,6,7,8-octahydro-4- thia-5-azaphenanthrene (2) and 4,8-dioxo-3,4,7,8-tetrahydro-2H,6H- [1,4]thiazepino[2,3,4-ij]quinoline (3). Analytical and spectral data are presented which support the structures proposed for these compounds. ��� Alternative synthesis of each heterocycle was achieved by using media other than polyphosphoric acid to cyclize the dicarboxylic acid (1). Phosphoryl chloride gave β-(4-oxo-2,3,4,5-tetrahydro-1,5- benzothiazepin-5-yl)propionic acid (4), which was cylodehydrated smoothly to the thiazepine (3). Concentrated sulphuric acid afforded β- (4-oxo-1,2,3,4-tetrahydroquinol-8-ylthio)propionic acid (6) which was converted into the thiazaphenanthrene (2) by polyphosphoric acid. ��� Bromination reactions and reduction with sodium borohydride of the thiazepine (3) are also described.


2021 ◽  
Vol 9 (11) ◽  
pp. 351-362
Author(s):  
Shilpi Srivastava ◽  

Complexes of bis(mercapto azoles) i.e. bis(mercapto triazoles), bis(mercapto thiadiazoles) and bis(mercapto oxadiazoles) (LH2) with manganese(III), iron(III) and cobalt(III) have been prepared in methanol in the presence of sodium hydroxide and binuclear products of the type Na[M(L)2(H2O)2] have been isolated. Tentative structural conclusions are drawn for these complexes based upon elemental analyses, electrical conductance, magnetic moment and spectral (electronic, infrared and 1H NMR) data. The thermal stability and mode of decomposition for the complexes have been studied by TG, DTA and DSC techniques. The antifungal, antiviral and antibacterial activities of the ligands and their corresponding complexes were also investigated.


2005 ◽  
Vol 3 (3-4) ◽  
pp. 289-297 ◽  
Author(s):  
A. K. Srivastava ◽  
O. P. Pandey ◽  
S. K. Sengupta

The reactions of bis(cyclopentadienyl)titanium(IV) dichloride with Schiff bases derived by condensing 2- amino-5-phenyl-1,3,4-thiadiazole with benzaldehyde (SPT), 4-nitrobenzaldehyde (SNT), 4-methoxybenzaldehyde (SMT), 2-hydroxybenzaldehyde (SSTH) or 2-hydroxyacetophenone (SATH) have been studied in refluxing tetrahydrofuran and complexes of types [Cp2TiCl(SB)]Cl (SB= SPT, SNT or SMT) and [Cp2Ti(SB')]Cl (SB'H= SSTH or SATH) have been isolated. Tentative structural conclusions are drawn for these reaction products based upon elemental analyses, electrical conductance, magnetic moment and spectral (UV-vis, IR and1H NMR) data. Studies were conducted to assess the growth-inhibiting potential of the complexes synthesized, and the ligands, against various fungal and bacterial strains.


2019 ◽  
Author(s):  
Chem Int

A series of novel 1, 3, 4-oxadiazole analogues was synthesized from cyclization of hydrazones of substituted 1-ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carbohydrazides were prepared from nalidixic acid. The structures of synthesized oxadiazole derivatives and their copper complexes were elucidated on the basis of FTIR, elemental analyses, 1H-NMR and atomic absorption spectral analysis. It was observed from spectral data that metal ligand ratio was 1:1 in all copper complexes and they were bidentate, coordination was found to be done through oxygen of 4-oxo group and nitrogen of oxadiazole ring. The synthesized compounds were further evaluated with biological activities and compared with parent hydrazones. Copper complexes possess antibacterial and antifungal activities better than the oxadiazoles while they have better antioxidant activity then copper complexes. Parent hydrazones were better in all biological activities than synthesized oxadiazoles.


1998 ◽  
Vol 63 (3) ◽  
pp. 363-370 ◽  
Author(s):  
Violetta Patroniak-Krzyminiewska ◽  
Wanda Radecka-Paryzek

The template reactions of 2,6-diacetylpyridine with 3,6-dioxaoctane-1,8-diamine in the presence of dysprosium(III), thulium(III) and lutetium(III) chlorides and erbium(III) perchlorate produce the complexes of 15-membered macrocyclic ligand with an N3O2 set of donor atoms as a result of the [1+1] Schiff base cyclocondensation. In contrast, analogous reactions involving the lighter lanthanide ions (lanthanum(III), samarium(III) and europium(III)) yield the acyclic complexes with terminal acetylpyridyl groupings as products of the partial [2+1] condensation. The complexes were characterized by spectral data (IR, UV-VIS, 1H NMR, MS), and thermogravimetric and elemental analyses.


Author(s):  
Süheyla Özbey ◽  
Nilgün Karalı ◽  
Aysel Gürsoy

AbstractIn this study 4-(3-coumarinyl)-3-benzyl-4-thi azolin-2-one 4-methylbenzylidenehydrazone 3 was synthesised. An independent proof of the thiazolylhydrazone structure of 3 was achieved by single crystal X-ray diffraction analysis. Elemental analyses and spectral data (IR,


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