Proton Magnetic Resonance Investigation of Some Weak Interactions Between Naphthalene and Alkyl Iodides in Carbon Tetrachloride

1971 ◽  
Vol 49 (10) ◽  
pp. 1771-1774
Author(s):  
R. Sahai ◽  
S. H. Lin
Keyword(s):  
Carbon Tetrachloride ◽  
Magnetic Resonance ◽  
Proton Magnetic Resonance ◽  
Weak Interactions ◽  
Chemical Shifts ◽  
Dipole Model ◽  
Resonance Investigation ◽  
Entropy Changes ◽  
Alkyl Iodides ◽  
Magnetic Resonance Investigation

A p.m.r. investigation of the interactions between naphthalene and alkyl iodides has been reported. The equilibria, the heats and the entropy changes for the complexation, and the chemical shifts of the acceptor protons in the pure complex have been determined. A crude dipole model for these interactions has been suggested.

Protonenresonanz-spektroskopische Untersuchungen am Chlor-, Brom- und Methylcyclobutadieneisentricarbonyl / A Proton Magnetic Resonance Investigation on Chloro-, Bromo- and Methyl-cyclobutadiene-irontricarbonyl

1974 ◽  
Vol 29 (3-4) ◽  
pp. 219-227 ◽  
Author(s):  
Hans Albert Brune ◽  
Hans Hanebeck ◽  
Gernot Horlbeck ◽  
Hans Hüther
Keyword(s):  
Magnetic Resonance ◽  
Proton Magnetic Resonance ◽  
Electron Distribution ◽  
Membered Ring ◽  
Bond Orders ◽  
Higher Symmetry ◽  
Resonance Investigation ◽  
Cyclic Diene ◽  
Magnetic Resonance Investigation ◽  
Single Bonds

Proton magnetic resonance spectra including all observable 13C-H-couplings have been measured for chloro-cyclobutadiene-irontricarbonyl.bromo-cyclobutadiene-irontricarbonyl and methyl-cyclobutadiene-irontricarbonyl. The results are discussed with respect to structure and bonding. The structure of a cyclic diene with alternating double and single bonds can be excluded for the four-membered ring of all three compounds. Instead the complex bonded cyclobutadiene contains an electron distribution of higher symmetry with — despite the influence of the substituent — nearly uniform bond orders.

The analysis of the proton magnetic resonance spectra of heteroaromatic systems. V. Diazanaphthalenes

1965 ◽  
Vol 18 (5) ◽  
pp. 707 ◽  
Author(s):  
PJ Black ◽  
ML Heffernan
Keyword(s):  
Carbon Tetrachloride ◽  
Magnetic Resonance ◽  
Long Range ◽  
Iterative Procedure ◽  
Proton Magnetic Resonance ◽  
Chemical Shifts ◽  
Direct Calculation ◽  
Coupling Constants ◽  
Dilute Solutions ◽  
Magnetic Resonance Spectra

The proton magnetic resonance spectra of the four isomeric diazanaphthalenes, quinoxaline, phthalazine, quinazoline, and cinnoline, all as dilute solutions in carbon tetrachloride and acetone, have been investigated at 100 Mc/s. The chemical shifts and coupling constants have been obtained by direct calculation or, where appropriate, by an iterative procedure. Long-range coupling constants between protons separated by five and six bonds have been observed.

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