scholarly journals The mass spectra of Schiff bases. II. Two deuterated species

1969 ◽  
Vol 22 (10) ◽  
pp. 2249 ◽  
Author(s):  
DJ Elias ◽  
RG Gillis
Keyword(s):  
Schiff Bases ◽  
Mass Spectra

scholarly journals Synthesis, Characterization and Antitumor Activity of Some New Oganotellurium Compounds Containing Azomethine Group, Part One

2016 ◽  
Vol 8 (1) ◽  
pp. 1464-1471 ◽  
Author(s):  
Rafid H. Al-Asadi ◽  
Tarik A. Fahad ◽  
Bahjat A. Saeed ◽  
Wasfi A. Al-Masoudi
Keyword(s):  
Antitumor Activity ◽  
Hydrazine Hydrate ◽  
Schiff Bases ◽  
Elemental Analysis ◽  
13C Nmr ◽  
Mass Spectra ◽  
The Other ◽  
Azomethine Group ◽  
Other Hand ◽  
Group Part

New tellurated schiff bases were synthesized by the reaction of the corresponding mercurated Schiff  bases compounds A1-A3 with tellurium tetrabromide in 1:1 mole ratio and  that  gave organyltellurium tribromides  A4-A6.  On the other hand, when mercurated schiff bases and tellurium tetrabromide brought  together in 2:1 mole ratio gave diorganyltellurium dibromides compounds A10-A12 followed by reduction with hydrazine hydrate gave new diorganyl tellurides A13-A15.  Reduction of compounds A4-A6 by  hydrazine hydrate gave new ditellurides A7-A9.  All compounds were characterized by elemental analysis, IR, 1H , 13C NMR, HSQC-NMR and mass spectra.  Invitro anti-tumor bioactivity of some compounds were tested. 

scholarly journals Synthetic, structural and antifungal studies of coordination compounds of Ru(III), Rh(III) and Ir(III) with tetradentate schiff bases

2006 ◽  
Vol 71 (8-9) ◽  
pp. 917-928 ◽  
Author(s):  
V.K. Sharma ◽  
Ankita Srivastava ◽  
Shipra Srivastava
Keyword(s):  
Spectral Data ◽  
Schiff Bases ◽  
Magnetic Moment ◽  
Coordination Compounds ◽  
Mass Spectra ◽  
Thermal Analyses ◽  
Agar Plate ◽  
Plate Method ◽  
Elemental Analyses ◽  
Fab Mass Spectra

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.

scholarly journals Synthesis of Some Salicylaldehyde-Based Schiff Bases in Aqueous Media

2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Sunita Bhagat ◽  
Nutan Sharma ◽  
Tejpal Singh Chundawat
Keyword(s):  
Microwave Irradiation ◽  
Schiff Bases ◽  
Mass Spectra ◽  
Aqueous Media ◽  
Thermal Conditions ◽  
Reaction Conditions ◽  
Step Procedure ◽  
One Step ◽  
Judicious Choice ◽  
Work Up

A new efficient and environmental friendly procedure for the synthesis of a series of salicylaldehyde-based schiff bases under microwave irradiation is described. The method is compared with the conventional method also. The present work involves condensation of salicylaldehyde with various aromatic amines in water under microwave irradiation. A judicious choice of the solvent and reaction conditions allowed the final products to be generated in excellent yields in a one-step procedure, whereas experiments under thermal conditions led to lower yields with tedious work-up. Microwave irradiation method gives advantages like reduction in reaction time, increase in conversion, reduced wastes, and good yields. The structures of synthesized compounds were confirmed by IR, 1HNMR, and Mass Spectra data.

scholarly journals Synthesis, Identification and Biological Activity of New Heterocyclic Compounds from Reaction of New Schiff-Bases with Phathalic Anhydride

2020 ◽  
Vol 8 (1) ◽  
pp. 12-18
Author(s):  
Alya A. Dawood ◽  
Shireen R. Mmohammed ◽  
Mohammed Mahmoud
Keyword(s):  
Acetic Acid ◽  
Schiff Bases ◽  
Heterocyclic Compounds ◽  
Mass Spectra ◽  
Glacial Acetic Acid ◽  
Biological Activities ◽  
Condensation Reaction ◽  
Aromatic Aldehydes ◽  
Heterocyclic Ring ◽  
Second Step

Series of new Schiff bases and their derivatives (Oxazepine) have been synthesized during two steps. The first step synthesis of imines derivatives (1-10) by the condensation reaction of 1, 7-diaminohepatane and 1,8-diaminooctane with different substituted aromatic aldehydes by using glacial acetic acid as catalyst. The second step includes reaction of the prepared Schiff bases derivatives with phathalic anhydride in dry benzene to obtain   seven-membered heterocyclic ring derivatives (11-15).  The biological activities of some prepared compounds were also studied against different kinds of bacteria. The new derivatives were confirmed by suing a range of experimental techniques including 1HNMR, 13C NMR, IR and Mass spectra.

Electron impact mass spectra of new acyclic and macrocyclic sulphur-containing Schiff bases

1985 ◽  
Vol 20 (12) ◽  
pp. 789-791 ◽  
Author(s):  
Pietro A. Vigato ◽  
Sergio Sitran ◽  
Dolores Fregona ◽  
Sergio Daolio ◽  
Pietro Traldi
Keyword(s):  
Electron Impact ◽  
Schiff Bases ◽  
Mass Spectra ◽  
Electron Impact Mass ◽  
Impact Mass

The mass spectra of Schiff bases. I. Simple fissions and rearrangements

1966 ◽  
Vol 19 (2) ◽  
pp. 251 ◽  
Author(s):  
DJ Elias ◽  
RG Gillis
Keyword(s):  
Double Bond ◽  
Electron Impact ◽  
Schiff Bases ◽  
Mass Spectra ◽  
Hydrogen Transfer ◽  
Molecular Ion ◽  
Ring Carbon ◽  
Carbon Bonds ◽  
Ring Nitrogen ◽  
Derivatives Of

Under electron impact, Schiff bases give a stable molecular ion which undergoes simple fission at the ring-nitrogen and ring-carbon bonds. Ortho substitution leads to ions derived from five-membered heterocycles. Derivatives of o-methoxy-benzaldehyde exhibit a two-hydrogen transfer with fission of the azomethine double bond to give the amine radical-ion.

scholarly journals Synthesis, Characterization and Antibacterial Activity of Novel Schiff Bases Derived from 4-Phenyl-2-aminothiazole and their Mn(II), Fe(II), Co(II), Ni(II) and Cu(II) Metal complexes

2011 ◽  
Vol 8 (4) ◽  
pp. 1556-1565 ◽  
Author(s):  
A. S. Thakar ◽  
K. S. Pandya ◽  
K. T. Joshi ◽  
A. M. Pancholi
Keyword(s):  
Antibacterial Activity ◽  
Metal Complexes ◽  
Schiff Bases ◽  
Mass Spectra ◽  
Uv Spectra ◽  
Assay Method ◽  
H Nmr ◽  
Ft Ir ◽  
Schiff Base Metal Complexes ◽  
C Nmr

Novel Schiff bases and their metal complexes were derived from some hetero cyclicβ-diketones with 4-phenyl-2-aminothiazole. All the synthesized compounds were confirmed their structure by Elemental analysis, FT-IR,1H NMR,13C NMR, Mass spectra, TGA analysis and UV spectra. All the compounds were tested for their antibacterial activity. Spectroscopic measurements suggest that all Schiff base metal complexes are of type ML2.(H2O)2(M=Mn, Fe, Co, Ni and Cu) and all the metal complexes shows moderate antibacterial activity in the agar cup assay method.

scholarly journals Synthesis, Characterization and Antibacterial Activity of Schiff Bases and their Metal Complexes Derived from 4-Acyl-1-phenyl-3-methyl-2-pyrazolin-5-ones and 2-Amino-4(4'-methylphenyl)-thiazole

2010 ◽  
Vol 7 (4) ◽  
pp. 1396-1406 ◽  
Author(s):  
A. S. Thakar ◽  
K. K. Singh ◽  
K. T. Joshi ◽  
A. M. Pancholi ◽  
K. S. Pandya
Keyword(s):  
Antibacterial Activity ◽  
Schiff Bases ◽  
Elemental Analysis ◽  
Mass Spectra ◽  
Nmr Spectra ◽  
Electrical Conductance ◽  
H Nmr ◽  
Infrared Spectral ◽  
Ft Ir ◽  
C Nmr

4-Acyl-1-phenyl-3-methyl-2-pyrazolin-5-ones condensed with 2-amino-4(4'-methylphenyl)-thiazole to form Schiff base. These Schiff bases from complexes of type ML22H2O (M=Mn, Fe, Co, Ni and Cu). Elemental analysis, magnetic susceptibility, electrical conductance, electronic and Infrared spectral data suggested octahedral structure for the complexes. All the compounds were tested for their antibacterial activity. The result indicates that the growth of the tested organism was inhibited by most of the compounds. These Schiff bases are characterized by elemental analysis, mass spectra,1H-NMR spectra,13C NMR spectra and FT IR spectra.

Mass spectra of nitrogen heterocycles. II. Pyridyl Schiff bases

1973 ◽  
Vol 26 (5) ◽  
pp. 1031
Author(s):  
EJ Halbert ◽  
RJ Goldsack ◽  
JG Wilson
Keyword(s):  
Schiff Bases ◽  
Mass Spectra ◽  
Pyridyl Ring ◽  
Fragmentation Pattern ◽  
Methyl Radical ◽  
Azomethine Group ◽  
Major Reaction ◽  
Electron Impact Mass ◽  
Methoxy Substituent ◽  
Impact Mass

A number of anils of pyridine aldehydes and benzylideneaminopyridines were used to study positional effects of aromatic substituents and heteroatom placement on electron impact mass spectra. The simple fragmentation pattern of aromatic Schiff bases was obtained with all 3- and 4-pyridyl compounds when the other aromatic ring was unsubstituted phenyl, or in the case of anils, had a chloro or 3-methoxy substituent. Marked changes were brought about by a pyridyl ring at either end of the azomethine group when the heterocyclic nitrogen was adjacent to it. Displacement and rearrangement reactions then became dominant. Methoxy substitution para to the azomethine in all anils studied gave loss of methyl radical as the major reaction.

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