Coordination Compounds of Substituted 1,10-Phenanthrolines and Related Dipyridyls. II. Complexes of Iron and 2,9-Dimethyl-1,10-phenanthroline

1962 ◽  
Vol 15 (2) ◽  
pp. 235 ◽  
Author(s):  
DB Fox ◽  
JR Hall ◽  
RA Plowman
Keyword(s):  
Solid State ◽  
General Formula ◽  
Infrared Spectra ◽  
Coordination Compounds ◽  
Magnetic Moments ◽  
Tetrahedral Complexes ◽  
Covalently Bound

A number of mono and bis(che1ate) complexes of iron(II) and 2,9-dimethyl-1,10-phenanthroline (dmp) have been isolated. The mono complexes are of general formula FedmpX2, where X=Cl, Br, I ; 2X=SO4. They are yellow to brown in colour except for the sulphato complex, which is pink. Conductivity and cryoscopic measurements indicate that the halogeno compounds are nonelectrolytes and monomeric. The magnetic moments range from 5.1 to 5.4 B.M. The evidence points to these compounds being four-coordinate tetrahedral complexes. The bis(che1ate)complexes are Fe(dmp)2(NO3)2(H2O)2 and Fe(dmp)2(NO3)(ClO4)(H2O)2, both yellow crystalline substances. They are 1 : 1 electrolytes in nitrobenzene and nitromethane. The magnetic moments are 5.2 B.M. for the dinitrate and 5.05 B.M. for the nitrate-perchlorate. According to their infrared spectra, each compound in the solid state appears to contain covalently bound nitrate and is most probably six-coordinate.

X-ray Structure Refinement and Vibrational Spectroscopy of Ca8Gd2 (PO4)6 O2

2013 ◽  
Vol 12 (10) ◽  
pp. 719-726
Author(s):  
R. Ayadi ◽  
Mohamed Boujelbene ◽  
T. Mhiri
Keyword(s):  
Solid State ◽  
General Formula ◽  
Vibrational Spectroscopy ◽  
Powder Diffraction ◽  
Infrared Spectra ◽  
Solid State Reaction ◽  
Structure Refinement ◽  
Unit Cell ◽  
Cell Group ◽  
X Ray

The present paper is interested in the study of compounds from the apatite family with the general formula Ca10 (PO4)6A2. It particularly brings to light the exploitation of the distinctive stereochemistries of two Ca positions in apatite. In fact, Gd-Bearing oxyapatiteCa8 Gd2 (PO4)6O2 has been synthesized by solid state reaction and characterized by X-ray powder diffraction. The site occupancies of substituents is0.3333 in Gd and 0.3333 for Ca in the Ca(1) position and 0. 5 for Gd in the Ca (2) position.  Besides, the observed frequencies in the Raman and infrared spectra were explained and discussed on the basis of unit-cell group analyses.

Transition metal acetates

1968 ◽  
Vol 46 (22) ◽  
pp. 3443-3446 ◽  
Author(s):  
D. A. Edwards ◽  
R. N. Hayward
Keyword(s):  
Solid State ◽  
Thermogravimetric Analysis ◽  
Transition Metal ◽  
Infrared Spectra ◽  
Magnetic Moments ◽  
Acetate Group ◽  
Visible Spectra

Some anhydrous transition metal acetates (Mn(II), Co(II), Cu(II), Ni(II), Zn(II), Ag(I), Mo(II), Ce(III), La(III)) have been prepared and their infrared spectra measured in the solid state. The infrared spectra have been related to established modes of bonding of the acetate group to metals. Thermal decompositions of the anhydrous acetates have been investigated by thermogravimetric analysis; magnetic moments and visible spectra have been measured.

Coordination compounds of substituted 1,10-Phenanthrolines and related dipyridyls. VIII. Complexes of silver and 2,9-Dimethyl-1,10-phenanthroline

1965 ◽  
Vol 18 (9) ◽  
pp. 1345 ◽  
Author(s):  
JR Hall ◽  
RA Plowman ◽  
HS Preston
Keyword(s):  
Aqueous Solutions ◽  
Organic Solvents ◽  
Infrared Spectra ◽  
Coordination Compounds ◽  
Molecular Weights ◽  
Low Solubility ◽  
Covalently Bound

Addition of 2,9-dimethyl-1,10-phenanthroline (dmp) in organic solvents to aqueous solutions of silver(1) salts yielded mono complexes represented by AgXdmp, where X = NO3, Cl, Br, I; 2X = SO4, and bis complexes Ag(dmp),Y, where Y = NO3, Cl04. Water of crystallization was present only in the sulphate. The mono complexes were empirically three-coordinate. Low solubility prevented the determination of molecular weights. Infrared spectra indicated that the polyatomic anions were covalently bound. The 1 : 1 electrolyte [Ag(dmp)(py)]ClO4 subsequently prepared seemed to be an example of three-coordination. The bis complexes were 1 : 1 electrolytes in nitrobenzene and were most likely tetrahedral.

scholarly journals X-ray Structure Refinement and Vibrational Spectroscopy of Ca8Gd2 (PO4)6 O2

2013 ◽  
Vol 12 (5) ◽  
pp. 719-726
Author(s):  
R. Ayadi ◽  
Mohamed Boujelbene ◽  
T. Mhiri
Keyword(s):  
Solid State ◽  
General Formula ◽  
Vibrational Spectroscopy ◽  
Powder Diffraction ◽  
Infrared Spectra ◽  
Solid State Reaction ◽  
Structure Refinement ◽  
Unit Cell ◽  
Cell Group ◽  
X Ray

The present paper is interested in the study of compounds from the apatite family with the general formula Ca10 (PO4)6A2. It particularly brings to light the exploitation of the distinctive stereochemistries of two Ca positions in apatite. In fact, Gd-Bearing oxyapatiteCa8 Gd2 (PO4)6O2 has been synthesized by solid state reaction and characterized by X-ray powder diffraction. The site occupancies of substituents is0.3333 in Gd and 0.3333 for Ca in the Ca(1) position and 0. 5 for Gd in the Ca (2) position.  Besides, the observed frequencies in the Raman and infrared spectra were explained and discussed on the basis of unit-cell group analyses.

Coordination compounds of 1,3-butadiene with anhydrous silver tetrafluoroborate

1967 ◽  
Vol 45 (12) ◽  
pp. 1329-1336 ◽  
Author(s):  
H. W. Quinn
Keyword(s):  
Solid State ◽  
Infrared Spectra ◽  
Coordination Compounds ◽  
Silver Ions ◽  
Crystalline Complexes Of

Two crystalline complexes of 1,3-butadiene with anhydrous silver tetrafluoroborate have been isolated and shown to have the stoichiometry [Formula: see text] and [Formula: see text]. On the basis of their infrared spectra, it has been suggested that in the solid state the 1:1 complex is polymeric in nature with alternating butadiene molecules and AgBF4 units in the chain and that the 2:3 complex is formed by bridging of butadiene molecules between silver ions in adjacent chains.

Metal complexes of hydrogenated Schiff bases

1967 ◽  
Vol 20 (10) ◽  
pp. 2077 ◽  
Author(s):  
MJ O'Conner ◽  
BO West
Keyword(s):  
Schiff Base ◽  
Solid State ◽  
Metal Complexes ◽  
Schiff Bases ◽  
Solid State Reaction ◽  
Magnetic Moments ◽  
Aryl Substituent ◽  
Infrared Measurements ◽  
Derivatives Of ◽  
Covalently Bound

N-Substituted o-hydroxybenzylamines formed by the hydrogenation of the C=N bond in N-arylsalicylideneimines were prepared, and found to be slightly stronger bases but much weaker acids than the corresponding Schiff base. They react with copper(II) acetate give crystalline derivatives of empirical constitution (copper(II) : ligand : acetate). Magnetic moments and infrared measurements indicate that the complexes are associated in the solid state. Reaction with copper(II) nitrate yields complexes of two types dependent on the aryl substituent. The o-tolyl derivative contains a covalently bound nitrato group while other derivatives have ionic nitrate groups. The quadridentate ligand N,N?-ethylenebis(o-hydroxybenzylamine) reacts readily with copper(II), nickel(II), and zinc(II) ions to give crystalline products which are probably associated in the solid state.

Coordination compounds of substituted 1,10-Phenanthrolines and related dipyridyls. V. Complexes of cobalt and 2,9-Dimethyl-1,10-phenanthroline

1965 ◽  
Vol 18 (5) ◽  
pp. 691 ◽  
Author(s):  
DB Fox ◽  
JR Hall ◽  
RA Plowman
Keyword(s):  
Absorption Spectra ◽  
Infrared Spectra ◽  
Coordination Compounds ◽  
Magnetic Moments ◽  
Visible Absorption

A series of complexes of cobalt(II) and 2,9-dimethyl-1,10-phenanthroline (dmp) has been prepared. Complexes of formula CoX2dmp (X = Cl, Br, I, KCS) are monomeric in acetone and camphor and non-electrolytes in nitrobenzene and nitromethane. The magnetic moments and visible absorption spectra favour the assignment of tetrahedral stereochemistry about the Co atom. Complexes containing 2 moles dmp per Co appear to have octahedral arrangements of ligands about the Co atom. These are of the type [CoNO3(H2O)dmp2]X, (X = NO3, ClO4, BPh4) and Co(NCS)2dmp2. The magnetic moments, visible and infrared spectra, and conductances in nitrobenzene and nitromethane support this conclusion. With other mono-dmp complexes (CoX2dmp, X = NO3, �SO4) and bis-dmp complexes {CoXdmp,ClO4,H2O (X = Cl, Br) ; Codmp2(ClO4)2}, stereochemical assignments could not be made.

Synthetic, Infrared, 1Hand 13CNMR Spectral Studies on N-(p-Substituted Phenyl)-p-Substituted Benzenesulphonamides, p-X’C6H4SO2NH- (p-XC6H4), where X’ or X = H, CH3, C2H5, F, Cl or Br

2004 ◽  
Vol 59 (4-5) ◽  
pp. 239-249
Author(s):  
B. Thimme Gowda ◽  
K. L. Jayalakshmi ◽  
Mahesha Shetty
Keyword(s):  
Solid State ◽  
General Formula ◽  
Infrared Spectra ◽  
Nmr Spectra ◽  
Chemical Shifts ◽  
Vibrational Frequencies ◽  
Spectral Studies ◽  
Benzene Rings ◽  
Electron Donating Groups ◽  
C Nmr

Thirty N-(p-substituted phenyl)-p-substituted benzenesulphonamides of the general formula, p-X’C6H4SO2NH(p-XC6H4), where X’ or X = H, CH3, C2H5, F, Cl or Br, are synthesised and their infrared spectra in the solid state and 1H and 13C NMR spectra in solution are measured. The N-H stretching vibrational frequencies, νN−H vary in the range 3334 - 3219 cm−1, while the asymmetric and symmetric SO2 vibrations appear in the ranges 1377 - 1311 cm−1 and 1182 - 1151 cm−1, respectively. The compounds exhibit S-N and C-N stretching vibrational absorptions in the ranges 937 - 898 cm−1 and 1310 - 1180 cm−1, respectively. There are no particular trends in the variation of these frequencies on substitution with either electron withdrawing or electron donating groups. The 1H and 13C chemical shifts of N-(p-substituted phenyl)-p-substituted benzenesulphonamides,are assigned to various protons and carbons of the two benzene rings. Further, incremental shifts of the ring protons and carbons due to -SO2NH(p-XC6H4) groups in the compounds of the formula, C6H5SO2NH(p-XC6H4), and p-X’C6H4SO2- and p-X’C6H4SO2NH- groups in the compounds of the formula, p-X’C6H4SO2NH(C6H5) are computed and used to calculate the 1H and 13C chemical shifts of the parallely substituted compounds of the general formula p-X’C6H4SO2NH(p-XC6H4). The computed values agree well with the observed chemical shifts. The above incremental shifts are found to correlate with the Hammett substituent parameters.

scholarly journals X-ray Structure Refinement and Vibrational Spectroscopy of Ca8Gd2 (PO4)6 O2

2009 ◽  
Vol 5 (2) ◽  
pp. 719-726
Author(s):  
R. Ayadi ◽  
Mohamed Boujelbene ◽  
T. Mhiri
Keyword(s):  
Solid State ◽  
General Formula ◽  
Vibrational Spectroscopy ◽  
Powder Diffraction ◽  
Infrared Spectra ◽  
Solid State Reaction ◽  
Structure Refinement ◽  
Unit Cell ◽  
Cell Group ◽  
X Ray

The present paper is interested in the study of compounds from the apatite family with the general formula Ca10 (PO4)6A2. It particularly brings to light the exploitation of the distinctive stereochemistries of two Ca positions in apatite. In fact, Gd-Bearing oxyapatiteCa8 Gd2 (PO4)6O2 has been synthesized by solid state reaction and characterized by X-ray powder diffraction. The site occupancies of substituents is0.3333 in Gd and 0.3333 for Ca in the Ca(1) position and 0. 5 for Gd in the Ca (2) position.  Besides, the observed frequencies in the Raman and infrared spectra were explained and discussed on the basis of unit-cell group analyses.

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