scholarly journals Rotational analysis of naphthol-aromatic ring complexes stabilized by electrostatic and dispersion interactions

Author(s):  
María Mar Quesada-Moreno ◽  
Melanie Schnell ◽  
Daniel A. Obenchain

For complexes involving aromatic species, substitution effects can influence the preferred geometry.

1998 ◽  
Vol 94 (3) ◽  
pp. 417-433 ◽  
Author(s):  
MARTIN VAN DER HOEF ◽  
PAUL MADDEN

2002 ◽  
Author(s):  
Donald F. Graves ◽  
Keith A. Hutchison ◽  
Trammell Neill

2019 ◽  
Vol 118 (1) ◽  
pp. 101-113
Author(s):  
SNIGDHA PREETHI R. V ◽  
Dr. M. VALLIAPPAN

The present study details the women employment and the overwhelming potential help for women to get the economic power and to change a gender connection on the employment market. Working women pick up a considerable measure of new skill and abilities associated with driving an organization as well as with personal improvement. Besides, they also conceded that more prominent support women in the market may contribute to defeat a stereotypical picture of woman as a mother and spouse. This is fought to be principally a result of structural shifts in the economy, changing effect of wage and substitution effects and an increase in instruction levels of women in the populace. Our results also suggest that development without any other person's information is not sufficient to increase women's economic activity, but instead the dynamics of development matter. These findings are especially imperative to help design policies to enhance women's work force cooperation rate so that India can take complete favorable position of its upcoming demographic dividend.


1987 ◽  
Vol 52 (7) ◽  
pp. 1780-1785 ◽  
Author(s):  
Petr Kuzmič ◽  
Libuše Pavlíčková ◽  
Milan Souček

Ultraviolet irradiation of the title compound I in the presence of butylamine gave predominantly products of nucleophilic photosubstitution by the amine, i.e., nitroanilines IIa and IIb. Besides, small amounts of products of hydrolysis (phenol III) and reductive coupling (azoxybenzene IV) were also formed. Comparison of the overall photolysis rate of I with that of 3,4-dimethoxy-1-nitrobenzene (V) indicates a minor loss of reactivity, most probably due to some deviation from coplanarity of the activating nitro group and the aromatic ring.


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