scholarly journals Syntheses and characterisation of chloro(h3-allyl) dicarbonylmolybdenum(II) complexes of chiral and achiral ditertiaryphosphines

2012 ◽  
Vol 10 (1) ◽  
pp. 165-171
Author(s):  
Joe Jesu Raj ◽  
Devendra Pathak ◽  
Pramesh Kapoor
Keyword(s):  
General Formula ◽  
Force Constant ◽  
Spectroscopic Techniques ◽  
Multinuclear Nmr ◽  
Precursor Complex ◽  
Elemental Analyses ◽  
Secular Equations

AbstractA series of the complexes of the general formula [ClMo(CO)2(η 3-C3H5)(P-P)], [where (P-P) = (m-CH3C6H4)2P(CH2)2PPh2 (m-t-dppe); cis-Ph2PCH=CHPPh2 (cis-diphos); Ph2PCH2CH2AsPh2 (arsaphos); Ph2P(CH2)4PPh2 (dppb); (±)-1,2-C6H4(PMePh)2 (rac-diphos); (2R,3R)Ph2PC*H(Me)C*H(Me)PPh2 (+)-chiraphos; (R,R)-Me2C(O)2{C*HCH2PPh2}2 (-)-diop] were synthesised by the reaction of the precursor complex [ClMo(CO)2(η 3-C3H5)(CH3CN)2] with the corresponding ditertiary phosphine in acetone. The complexes were isolated as yellow to orange air-stable solids and characterised by elemental analyses, FTIR and multinuclear NMR [1H, 31P{1H}] spectroscopic techniques. The carbonyl force constant values were calculated by Cotton and Kraihanzel approximate secular equations using ν C≡O stretching frequencies observed in the FTIR and these were found to be 14.30–14.59 mdyne 0-A−1 and 0.23–0.70 mdyne Å−1 for K1 and Ki respectively. Spectroscopic evidences have confirmed cis-octahedral structures for the synthesized complexes.

Oxa-azonia-boratacyclopentanes by Insertion of Dimethylaminobis(trifluoromethyl)borane into Epoxides

1993 ◽  
Vol 48 (7) ◽  
pp. 935-939 ◽  
Author(s):  
Hans Bürger ◽  
Thomas Hagen ◽  
Gottfried Pawelke
Keyword(s):  
General Formula ◽  
Mass Spectra ◽  
Multinuclear Nmr ◽  
Elemental Analyses

Dimethylaminobis(trifluoromethyl)borane, (CF3)2BNMe2 (A), reacts with epoxides of the general formula to yield five-membered heterocycles(CF3)2, R = Me (1), CH,F (2), CF3 (3), Et (4), Bz (5). With R = Ph a 1:2 mixture of the isomers (CF3)2O (6a) and (CF3)2 (6b) is obtained. To the contrary, and A form the borane-dimethylamine adduct (H2C=CMe—CH2-O)(CF3)2B • NHMe2 (7). The compounds have been characterized by elemental analyses, multinuclear NMR, IR and mass spectra.

Benzimidazole Derivatives as Potential Antimicrobial and Antiulcer Agents: A Mini Review

2019 ◽  
Vol 19 (16) ◽  
pp. 1292-1297 ◽  
Author(s):  
Ali Mohd Ganie ◽  
Ayaz Mahmood Dar ◽  
Fairooz Ahmad Khan ◽  
Bashir Ahmad Dar
Keyword(s):  
Cell Lines ◽  
Cancer Cell ◽  
1H Nmr ◽  
13C Nmr ◽  
Benzimidazole Derivatives ◽  
Spectroscopic Techniques ◽  
One Pot ◽  
Biological Screening ◽  
Elemental Analyses ◽  
Characterization Studies

:Here in we report the number of strategies for the synthesis of differently substituted benzimidazole derivatives. The protocols involved in the syntheses of these derivatives were one-pot or multi-component. The characterization studies of these derivatives were carried by using different spectroscopic techniques (1H NMR, 13C NMR and MS) and elemental analyses. The biological screening studies revealed that these benzimidazole derivatives show potential antibacterial as well as antifungal behavior. These benzimidazole derivatives not only depicted potential antiulcer properties but also showed moderate to good anticancer/cytotoxic behavior against different cancer cell lines.

Basic Chromium(III) Carboxylates: Reactions of Chromium(III) Chloride with Some Carboxylic Acids

1979 ◽  
Vol 34 (10) ◽  
pp. 1369-1372 ◽  
Author(s):  
Ramesh Kapoor
Keyword(s):  
Acetic Anhydride ◽  
General Formula ◽  
Carboxylic Acids ◽  
Magnetic Measurements ◽  
Molar Conductance ◽  
Strong Affinity ◽  
Elemental Analyses

Abstract Anhydrous chromium(III) chloride reacts with pure carboxylic acids (RCOOH where R = CH3, C2H5, n-C3H7, CH2Cl, CHCl2 and CCl3) to give basic trinuclear chromium(III) carboxylates of the general formula [Cr3O(OOCR)6]+Cl-. The reaction of CrCl3 with acetic anhydride, however, gives a partially substituted product, CrCl(OOCCH3)2.The formation of basic carboxylates has been attributed to the strong affinity of Cr3+ ions for water that they can abstract it even from pure carboxylic acids. Their addition compounds with ammonia have also been prepared. The compounds have been characterized by their elemental analyses, IR, molar conductance and magnetic measurements.

Structure Determination of 3,5-Biscyclohexylidene-1,2,4-trithiolane / Structure Determination of 3,5-Biscyclohexylidene-1,2,4-trithiolane

1980 ◽  
Vol 35 (8) ◽  
pp. 1015-1018 ◽  
Author(s):  
Werner Winter ◽  
Hanspeter Bühl ◽  
Herbert Meier
Keyword(s):  
General Formula ◽  
Structure Determination ◽  
Title Compound ◽  
Direct Methods ◽  
Spectroscopic Techniques ◽  
Space Group ◽  
X Ray ◽  
Cell Parameters ◽  
Final Structure

Abstract Fragmentation of 1,2,3-thiadiazoles (1) leads to the compounds 5 - 8 with an increasing proportion of sulphur. Numerous structural possibilities exist for the products 7 with the general formula (R2C2)2S3. The number of proposals can be reduced by spectroscopic techniques, but the final structure determination is accomplished by an X-ray analysis of the title compound 7a. 7a crystallizes in the space group P21/c (Z = 4) with cell parameters of a = 9.714(1), b = 16.188(8), c = 9.149(2) Å and β = 98.93(1)°. The structure is solved by direct methods and refined to R = 0.053 with 1955 diffractometer data (I ≥ 2σ(I)). The trithiolane ring has a puckered conformation and the whole molecule shows nearly perfect C2-symmetry, which is not required crystallographically.

Potential bioactive mononuclear diorganotin(IV) phenoxyacetohydroxamate complexes: synthesis, characterization and antimicrobial evaluation

2018 ◽  
Vol 0 (0) ◽  
Author(s):  
Vineet Kumar Choudhary ◽  
Abhishek Kumar ◽  
Neeraj Sharma
Keyword(s):  
Antimicrobial Agents ◽  
Salmonella Typhi ◽  
Molar Ratio ◽  
Distorted Octahedral Geometry ◽  
Spectroscopic Techniques ◽  
Concentration Method ◽  
Distorted Octahedral ◽  
Elemental Analyses ◽  
Antimicrobial Evaluation

AbstractThe new diorganotin(IV) complexes of composition [Me2Sn(C6H5OCH2CONHO)2](I) and [n-Bu2Sn(C6H5OCH2CONHO)2](II) have been synthesized by the reactions of Me2SnCl2andn-Bu2SnCl2with potassium phenoxyacetohydroxamate (PhOAHK=C6H5OCH2CONHOK) in 1:2 molar ratio in methanol and benzene solvent medium and characterized by elemental analyses and spectroscopic techniques (infrared,1H nuclear magnetic resonance and mass spectrometry). The [O,O coordination] through carbonyl and hydroxamic oxygen atoms and distorted octahedral geometry around the mononuclear tin has been inferred. The electrochemical behavior of complexes studied by the cyclic voltammetric technique has shown quasi-irreversible two-step reduction from tin (IV) to tin (II). Thermal behavior of complexes studied by the thermogravimetric technique in N2atmosphere has yielded SnO as the decomposition product. Thein vitroantimicrobial activity assays against various pathogenic Gram-negative bacteria, namely,Salmonella typhi,Escherichia coli; Gram-positiveBacillus cereusandStaphylococcus aureusand fungiAspergillus nigerandAlternaria alternataby the minimum inhibitory concentration method have shown their potential as promising antimicrobial agents compared to the respective standard chloramphenicol and nystatin drugs.

Chemistry of Alkoxo Complexes, Part III *Synthesis and Characterization of Some Mono(carboxylato)mono (alkoxo)nickel(II) Complexes

1979 ◽  
Vol 34 (3) ◽  
pp. 459-463 ◽  
Author(s):  
B. P. Baranwal ◽  
G. K. Parashar ◽  
R. C. Mehrotra
Keyword(s):  
Molecular Weight ◽  
Magnetic Susceptibility ◽  
General Formula ◽  
Synthesis And Characterization ◽  
Probable Structure ◽  
Equimolar Ratio ◽  
Elemental Analyses ◽  
Infra Red ◽  
Interchange Reactions

AbstractA number of mono(carboxylato)mono(alkoxo)nickel(II) complexes of the general formula, Ni(OR)(OOCR′), (with R′ = C13H27, C15H35 and C17H35) have been synthesized (where R = Me and Pri) by the reactions of nickel methoxide and isopropoxide with the respective carboxylic acids in equimolar ratio and (where R = Et and But) by alcohol interchange reactions. A study of the molecular weight, infra-red and electronic reflectance spectra and magnetic susceptibility in addition to elemental analyses has been carried out to throw some light on the probable structure of these derivatives.

scholarly journals Chemistry and Biological Evaluation of Some New Triazolopyrimidine Derivatives Containing Isopropyl Group

2019 ◽  
pp. 390-396
Author(s):  
Janaki H. Chauhan ◽  
Haresh K. Ram
Keyword(s):  
Antifungal Activity ◽  
1H Nmr ◽  
Biological Evaluation ◽  
Spectroscopic Techniques ◽  
Efficient Synthesis ◽  
Antibacterial And Antifungal Activity ◽  
Isopropyl Group ◽  
Elemental Analyses ◽  
Antibacterial And Antifungal

An efficient Synthesis of a novel series of N,7-bis(substitutedphenyl)-4,7-dihydro-5-isopropyl-[1,2,4]triazolo-[1,5-a]pyrimidine-6-carboxamide (4a-j) was accomplished from N-(substituedphenyl)-4-methyl-3-oxopentanamide, 3-amino-1,2,4-triazole and different aldehyde reflex 20 min with DMF and then after the cooling product was obtained. All the recently synthesized compounds were characterized by the Mass, IR, 1H-NMR and mass spectroscopic techniques and by elemental analyses. The newly synthesized compounds were assessed for their antibacterial and antifungal activity.

scholarly journals Synthesis, crystal structure, and theoretical studies of a macrocyclic silver(I) complex of imino-pyridyl Schiff base ligand

2021 ◽  
Vol 12 (3) ◽  
pp. 248-255
Author(s):  
Jahangir Mondal ◽  
Meman Sahu ◽  
Bhaskar Sharma ◽  
Rakesh Ganguly ◽  
Shubhamoy Chowdhury ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Complex I ◽  
Average Distance ◽  
Spectroscopic Techniques ◽  
Triclinic Space Group ◽  
X Ray ◽  
Elemental Analyses ◽  
Photophysical Studies ◽  
Pyridyl Ligand

The synthesis and characterization of an imino-pyridyl ligand N,N'-(butane-1,4-diyl)bis(1-(pyridin-2-yl)methanimine) (L) and its Ag(I)ClO4 complex (I) by various spectroscopic techniques and elemental analyses is presented in this study. X-ray single crystal structure of complex I revealed that in complex I, each Ag(I) ion is tetra coordinated with two pyridine N-atoms and two imine N-atoms of the ligand L, forming a macrocyclic dimeric Ag(I) grid. In the macrocyclic dimer complex I, Ag-Ag separation along the chain is 5.318 Å. The Ag-Npy average distance is 2.396 Å and that of the Ag-Nim is 2.257 Å. The macrocyclic dimer complex I is supramolecularly arranged by π-stacking interactions. Computational, Hirshfeld surface analysis and photophysical studies on ligand L and complex I have also been performed. Crystal data for C32H36Ag2Cl2N8O8 (M =947.33 g/mol): Triclinic, space group P-1 (no. 2), a = 9.1714(12) Å, b = 10.4373(14) Å, c = 10.8297(14) Å, α = 112.317(3)°, β = 91.391(3)°, γ = 92.353(3)°, V = 957.3(2) Å3, Z = 1, T = 293.15 K, μ(MoKα) = 1.220 mm-1, Dcalc = 1.643 g/cm3, 10248 reflections measured (4.07° ≤ 2Θ ≤ 53.098°), 3966 unique (Rint = 0.0280, Rsigma = 0.0331) which were used in all calculations. The final R1 was 0.0722 (I > 2σ(I)) and wR2 was 0.2229 (all data).

scholarly journals Synthesis, Characterization and Antiproliferative Activity of the Co(II), Ni(II), Cu(II), Pd(II) and Pt(II) Complexes of 2-(4-Thiazolyl)Benzimidazole (Thiabendazole)

2001 ◽  
Vol 8 (4) ◽  
pp. 189-194 ◽  
Author(s):  
Marek Z. Wisniewski ◽  
Tadeusz Glowiak ◽  
Adam Opolski ◽  
Joanna Wietrzyk
Keyword(s):  
Breast Cancer ◽  
General Formula ◽  
Magnetic Measurements ◽  
Human Cancer ◽  
Urinary Bladder Carcinoma ◽  
X Ray ◽  
Human Cancer Cell Lines ◽  
Elemental Analyses ◽  
Mcf 7

Complexes of 2-(4-thiazolyi)benzimidazole (thiabendazole, THBD) with Co(II), Ni(II), Cu(ll) of general formula ML2(NO3)2 H2O and complexes of Pd(II) and Pt(II) of general formula ML2Cl2 H2O have been obtained and characterized by elemental analyses, IR and far IR spectroscopy and magnetic measurements. The X-ray crystal structure of the copper(II) complex has been determined. The in vitro cell proliferation inhibitory activity of these compounds was examined against human cancer cell lines A 549 (lung carcinoma), HCV-29 T (urinary bladder carcinoma), MCF-7 (breast cancer), T47D (breast cancer), MES-SA (uterine carcinoma) and HL-60 (promyelocytic leukemia). Pt-THBD has been found to exhibit an antileukemic activity of the HL-60 line cells matching that of an arbitrary criterion.

Chelates of nickel(II) and copper(II) with tridentate Schiff base formed by the condensation of S-benzyldithiocarbazate with benzoin

1978 ◽  
Vol 56 (15) ◽  
pp. 2000-2002 ◽  
Author(s):  
M. T. H. Tarafder ◽  
M. Akbar Ali
Keyword(s):  
Schiff Base ◽  
Spectral Data ◽  
General Formula ◽  
Schiff Base Ligand ◽  
Nickel Complexes ◽  
Planar Structure ◽  
Spectral Studies ◽  
Square Planar ◽  
Elemental Analyses ◽  
Tridentate Schiff Base

New complexes with the Schiff base ligand derived from S-benzyldithiocarbazate (NH2—NH—CSSCH2C6H5) have been prepared and characterized by elemental analyses, magnetic, conductometric, ir, and electronic spectral studies. The tridentate ONS Schiff base S-benzyl-β-N-(phenyl, phenylhydroxymethyl)methylenedithiocarbazate gave mono-ligand complexes with Ni(II) and Cu(II) having the general formula [MligandX] (M = Ni(II) and Cu(II); X = NO3, Cl, Br, NCS). A proposed square-planar structure for the nickel complexes is supported by magnetic and spectral data. A square-planar structure is also suggested for Cu(II) complexes. The ir results give evidence of the different bondings present in the complexes.

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