The Inductive Effect and Chemical Reactivity. IV. Dipole Moments of Halogen Derivatives of Aliphatic Hydrocarbons1

1956 ◽  
Vol 78 (16) ◽  
pp. 3932-3936 ◽  
Author(s):  
Richard P. Smith ◽  
Earl M. Mortensen
1982 ◽  
Vol 47 (11) ◽  
pp. 2946-2960 ◽  
Author(s):  
Antonín Trka ◽  
Alexander Kasal

Partial EI-mass spectra of 3β-hydroxy- and 3β-acetoxy-5α-cholestanes substituted in positions 5α-, 6β- or 5α,6β- with a hydroxyl group or halogen atoms (fluorine, chlorine, bromine) are presented. The molecular ions of 5α,6β-disubstituted derivatives of 3β-hydroxy-5α-cholestane (or of its 3-acetate) are considerably more stable than the corresponding monosubstituted derivatives if at least one of the pair of the vicinal substituents is chlorine or fluorine. This increase in stability, most striking in 5α- and 6β-fluoro compounds, is explained by the inductive effect.


1968 ◽  
Vol 8 (5) ◽  
pp. 829-832
Author(s):  
V. I. Stanko ◽  
A. I. Echeistova ◽  
I. S. Astakhova ◽  
A. I. Klimova ◽  
Yu. T. Struchkov ◽  
...  

2018 ◽  
Vol 4 (1) ◽  
Author(s):  
Jamie S. Ritch

Abstract Chalcogenated derivatives of N-heterocyclic carbene ligands have received increasing attention due to their diverse chemical reactivity and potential applications in fields such as medicine and materials chemistry. This chapter summarizes the synthetic methods for the preparation of cyclic heavy chalcogenoureas featuring heterocyclic cores and explores their diverse coordination chemistry with p- and d-block metals.


Author(s):  
Yu. V. Kolodyazhnyi ◽  
V. A. Vasnev ◽  
I. A. Lapin ◽  
G. A. Alieva ◽  
M. G. Keshelava ◽  
...  

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