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کاربرد نوع شرط:
- جایگاه : پژوهشی
- مجله: Inorganic Chemistry Research
- نوع مقاله: Journal Article
- کلمات کلیدی: thermodynamic parameters,Schiff base Complexes,Tetraaza Schiff base,Formation constants,Free energy
- چکیده:
- چکیده انگلیسی: Some new symmetrical tetraaza Schiff base ligands containing 2-quinolinecarboxaldehyde moiety formed from condensation reaction of 2-quinolinecarboxaldehyde and o-phenylenediamine derivatives, such as N, Nˊ-bis(2-quinolylmethylidene)-4-methoxy-1, 2-phenylenediimine (L1), N, Nˊ-bis(2-quinolylmethylidene)-4-methy-1, 2-phenylenediimine (L2), N, Nˊ-bis(2-quinolylmethylidene)-4-chloro-1, 2-phenylenediimine (L3), N, Nˊ-bis(2-quinolylmethylidene)-4-carboxylic-1, 2-phenylenediimine (L4), N, Nˊ-bis(2-quinolylmethylidene)-4-nitro-1, 2-phenylenediimine (L5), and their Ni(II), Cu(II), Zn(II) complexes, have been synthesized. The ligands and their metal complexes have been characterized by molar conductance, elemental analysis, IR, 1H-NMR and UV-Vis spectroscopy. The formation constant and the free energy of the complexes were determined using electronic spectroscopic titration at constant ionic strength 0.1 M (NaClO4), at 25°C in MeOH solvent. The comparison of the formation constants and the thermodynamic parameters show that the trend of complex formation toward a given ligand is as follows: L2 > L1 > L3 > L5 > L4 . The trend for complex formation of the metal ions with a given ligand is as follows: Zn (II) > Cu (II) > Ni (II).
- انتشار مقاله: 01-08-1393
- نویسندگان: Alison Zamanpour,Mozaffar Asadi,Ghodratollah Absalan
- مشاهده
- جایگاه : پژوهشی
- مجله: Iranian Journal of Chemistry and Chemical Engineering
- نوع مقاله: Journal Article
- کلمات کلیدی: charge transfer,Equilibrium parameters,Weak molecular complexes,Modified Cresswel- Allred method,Scatchard-Foster-Fyfe method
- چکیده:
- چکیده انگلیسی: The charge transfer (CT) complex formation of benzonitrile as acceptor with the aromatic donors o-, m-, p-xylene and ethylbenzene in CCl4 solutions is investigated by chemical shift measurements relative to an external reference. The equilibrium parameters, Q and DAD of their weak molecular complexes, as found numerically modified Cresswel- Allred (C-A) method, is compared with graphically Scatchard-Foster-Fyfe (Sc-F-F) method.
- انتشار مقاله: 20-05-1380
- نویسندگان: Mahmood Niad,Mozaffar Asadi
- مشاهده
- جایگاه : پژوهشی
- مجله: Iranian Journal of Chemistry and Chemical Engineering
- نوع مقاله: Journal Article
- کلمات کلیدی: Kinetics,Mechanism,Mixed solvents,Substitution reactions,Co(III) complexes,Anion interchanges
- چکیده:
- چکیده انگلیسی: The kinetics and mechanisms of the substitution reactions of trans-[Co(en)2CNCl]+ with unidentate anions, , CN¯, I¯, , Br¯ and SCN¯ in 60% v/v DMF-H2O binary solvent at 40.0±0.2 °C were studied spectrophotometrically. An Id mechanism was assigned for the replacement of chlorine by , CN¯ and I¯, an Ia one for the entry of and SCN¯, and a D mechanism for Br¯ entry. Comparing the interchange rate constants, ki, values has led to the following trend of reactivity of the anions toward the given substrate: The replacement of chlorine by the anions proceeded with a complete retention of configuration.
- انتشار مقاله: 07-08-1376
- نویسندگان: Mozaffar Asadi,Hassan Rajabloo
- مشاهده
- جایگاه : پژوهشی
- مجله: Iranian Journal of Chemistry and Chemical Engineering
- نوع مقاله: Journal Article
- کلمات کلیدی: Mixed solvent,Triorganotin chloride,Adduct compounds,stannane chlorotriaryl,Acceptor property
- چکیده:
- چکیده انگلیسی: The equilibrium constant of adduct formation between some triorganotin chloride of the type R3SnCl (R=C6H5, p-CH3C6H4, n-CH3)CH2)3, C6H5-CH2 and Lewis bases Cl¯, Br¯, and I¯, were measured in 50% v/v ethanol-water solvent spectrophotometrically. The average equilibrium constant values for the systems studied shows the following acceptor trend of tin(IV) in the triorganotin chlorides: p-tolyl > n-butyl > Phenyl > benzyl The influence of the organic moieties on the acceptor property of tin(IV) is discussed..
- انتشار مقاله: 21-04-1371
- نویسندگان: Mozaffar Asadi,Gasi Abdul Wahab Derwich
- مشاهده
- جایگاه : پژوهشی
- مجله: Inorganic Chemistry Research
- نوع مقاله: Journal Article
- کلمات کلیدی: thermodynamic parameters,Schiff base Complexes,Tetraaza Schiff base,Formation constants,Free energy
- چکیده:
- چکیده انگلیسی: Some new symmetrical tetraaza Schiff base ligands containing 2-quinolinecarboxaldehyde moiety formed from condensation reaction of 2-quinolinecarboxaldehyde and o-phenylenediamine derivatives, such as N, Nˊ-bis(2-quinolylmethylidene)-4-methoxy-1, 2-phenylenediimine (L1), N, Nˊ-bis(2-quinolylmethylidene)-4-methy-1, 2-phenylenediimine (L2), N, Nˊ-bis(2-quinolylmethylidene)-4-chloro-1, 2-phenylenediimine (L3), N, Nˊ-bis(2-quinolylmethylidene)-4-carboxylic-1, 2-phenylenediimine (L4), N, Nˊ-bis(2-quinolylmethylidene)-4-nitro-1, 2-phenylenediimine (L5), and their Ni(II), Cu(II), Zn(II) complexes, have been synthesized. The ligands and their metal complexes have been characterized by molar conductance, elemental analysis, IR, 1H-NMR and UV-Vis spectroscopy. The formation constant and the free energy of the complexes were determined using electronic spectroscopic titration at constant ionic strength 0.1 M (NaClO4), at 25°C in MeOH solvent. The comparison of the formation constants and the thermodynamic parameters show that the trend of complex formation toward a given ligand is as follows: L2 > L1 > L3 > L5 > L4 . The trend for complex formation of the metal ions with a given ligand is as follows: Zn (II) > Cu (II) > Ni (II).
- انتشار مقاله: 01-08-1393
- نویسندگان: Alison Zamanpour,Mozaffar Asadi,Ghodratollah Absalan
- مشاهده