Dipole moment, Kerr constant, Cotton-Mouton constant and conformation of 1,4-dithiin

1982 ◽  
Vol 35 (11) ◽  
pp. 2335 ◽  
Author(s):  
D Mirarchi ◽  
L Phillips ◽  
GLD Ritchie

Measurements of the infinite-dilution dipole moment, molar Kerr constant and molar Cotton-Mouton constant of 1,4-dithiin dissolved in cyclohexane and carbon tetrachloride at 25�C are reported and analysed to provide information concerning the solution-state conformation, the polarizability anisotropy and the magnetic anisotropy of this molecule.

1981 ◽  
Vol 34 (11) ◽  
pp. 2253 ◽  
Author(s):  
MP Brereton ◽  
MK Cooper ◽  
GR Dennis ◽  
GLD Ritchie

Measurements of the infinite-dilution molar Kerr constant, field-gradient birefringence constant and Cotton-Mouton constant of carbon diselenide as a solute in carbon tetrachloride at 298 K are reported. From an analysis of the observations, the molecular quadrupole moment, Θ, and the magnetic anisotropy, ΔX, emerge as (+15.4 � 2.7) × 10-40 Cm2 and (-19.6 � 2.6) × 10-5 J T-2 mol-1, respectively. Trends in these and related electric and magnetic properties are considered for the sequence of six linear triatomic molecules of formula XCY (X,Y = O,S,Se).


1987 ◽  
Vol 40 (3) ◽  
pp. 619 ◽  
Author(s):  
MJ Aroney ◽  
RJW LeFevre ◽  
RK Pierens ◽  
HJ Stootman ◽  
MGM Yong

Measurements are reported of the infinite-dilution dipole moments and molar Kerr constants of dimethyl sulfone and of the four aryl methyl sulfones p-XC6H4S(02)CH3 (X = H, Cl, Br or NO2) dissolved in carbon tetrachloride or dioxan at 298 K and under light of 589 nm. The experimental data are analysed to obtain information on the solution-state conformations in relation to steric and electromeric effects operative between the aryl and methanesulfonyl groups.


1982 ◽  
Vol 35 (5) ◽  
pp. 869 ◽  
Author(s):  
GLD Ritchie ◽  
J Vrbancich

Measurements of the infinite-dilution molar Cotton-Mouton and Kerr constants of 12 non-dipolar 1,3,5-tri- and hexa-substituted benzenes as solutes in carbon tetrachloride at 298 K are reported. Some of the experimental results are in notable disagreement with earlier determinations made on equipment of much lower sensitivity. Although the magnetic anisotropies derived for the tri-substituted benzenes are concordant with other observed or predicted values, those for the hexa-substituted benzenes are generally very much larger than expected. It is suggested, in explanation, that relatively large and strongly anisotropic atomic polarizabilities may cause the ratio of the static to the high-frequency polarizability anisotropy to be considerably smaller in the hexa-substituted benzenes than in benzene; in addition, there may be significant temperature independent contributions to the magnetic birefringences of these molecules.


1972 ◽  
Vol 25 (12) ◽  
pp. 2615 ◽  
Author(s):  
HH Huang ◽  
ELK Tan

The molar Kerr constant (35 x 10-12) and dipole moment (2.29 D) of 1,3-dichloroacetone in carbon tetrachloride are shown to be compatible with an equilibrium mixture of planar cis/non-planar gauche (6) and non-planar gauche/non-planar gauche (8) conformers with the latter predominating.


1964 ◽  
Vol 17 (10) ◽  
pp. 1098 ◽  
Author(s):  
FFvre RJW Le ◽  
BJ Orr

The magnitudes of dipole moment and molar Kerr constant of 1,2-dichloroethane as solute in carbon tetrachloride, previously recorded by Aroney, Izsak, and Le F�vre, are discussed in relation to internal rotation in the molecule. The results are found to be consistent with a mixture consisting of 31.3% of gauche-isomer and 68.7 % of trans-isomer. Estimation of the potential energy barriers restricting intramolecular rotation is attempted and the results found to be satisfactory.


1982 ◽  
Vol 35 (11) ◽  
pp. 2341 ◽  
Author(s):  
D Mirarchi ◽  
GLD Ritchie

Infinite-dilution dipole moments (1030p/Cm) and molar Kerr constants (1027mK/m5 V-2 mol-1) for 1-pivaloylnaphthalene (8.83,-490) and 2-pivaloylnaphthalene (9.24, 218) as solutes in carbon tetrachloride at 25�C are reported and analysed to yield the dihedral angles between the Car-CO-C and naphthyl planes as 90 � 10� and 53 � 8�, respectively.


1980 ◽  
Vol 33 (12) ◽  
pp. 2597 ◽  
Author(s):  
PH Gore ◽  
IG John ◽  
RK Pierens ◽  
GLD Ritchie

Experimental dipole moments and molar Kerr constants are reported and analysed for di(pyridin-4-yl), di(pyridin-3-yl) and di(pyridin-2-yl) ketone as solutes in carbon tetrachloride or cyclohexane at 298 K. The preferred conformation of di(pyridin-4-yl) ketone is found to be very similar to those previously deduced for benzophenone and several 4,4'- disubstituted benzophenones. For di(pyridin-3-yl) and di(pyridin-2-yl) ketone three analogous conrotatory structures having different relative dispositions of the nitrogen atoms are considered. In the case of di(pyridin-3-yl) ketone the cis-trans and trans-trans arrangements are approximately equally abundant, but for di(pyridin-2-yl) ketone there is a strong preference for the trans-trans conformation.


1979 ◽  
Vol 34 (3) ◽  
pp. 369-374 ◽  
Author(s):  
M. Kunst ◽  
D. van Duijn ◽  
P. Bordewijk

Abstract Analysis of infrared hydroxyl multimer absorbances of dilute solutions of cholesterol in carbon tetrachloride as a function of the monomer absorbance strongly favours the interpretation of the association of this alcohol with a monomer-dimer-tetramer model up to a molar fraction of 0.012. This model also explains very well the concentration dependence of the apparent dipole moment. Equilibrium constants and dielectric parameters have been determined. Suggestions about the structure of the various associates are made.


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