Preferential water remediation of cationic dyes using structurally engineered novel organoselenium based self-assembled constructs

Author(s):  
Surinder Kaur Brar ◽  
Sanjeev Kumar ◽  
Aman K. Bhasin ◽  
K.k Bhasin ◽  
Rohit K. Sharma

Selenide derivatives of imidazo[1, 2-a]pyridyl heterocyclic system have been investigated for their potential to generate novel and diverse self-assembled architectures. The effect of structural modification as well as insertion of...

Author(s):  
Hoseon You ◽  
Austin Jones ◽  
Boo Soo Ma ◽  
Geon-U Kim ◽  
Seungjin Lee ◽  
...  

In this study, two wide-bandgap PM7 polymer derivatives are developed via simple structural modification of the fused-accepting unit by incorporating ester groups on terthiophene at different positions (i.e., two ester...


INEOS OPEN ◽  
2021 ◽  
Vol 4 ◽  
Author(s):  
O. N. Gorunova ◽  
◽  
N. A. Bystrova ◽  
K. A. Kochetkov ◽  
◽  
...  

The possibility of structural modification of thiohydantoin derivatives via amidoalkylation under the action of a range of cyclic hemiamidals is demonstrated. The suggested approach provides, in particular, unsymmetrical nitrogen-containing bis-heterocyclic systems with pharmacologically relevant groups that are difficult to obtain by other methods.


2020 ◽  
Vol 24 (9) ◽  
pp. 1503-1507
Author(s):  
S.O. Okopi ◽  
L.M. Affiku

Methyl eugenol is a naturally occurring substance found in the essential oils of several plant species. It is a cheap and abundant material with a rather limited interest as perfuming ingredient. This research investigated the structure-odour relationship of methyl eugenol and its derivatives, focusing on the chemical transformation of the double bond to hydroxyether derivatives in a controlled manner. Two derivatives 2-(4-ethyl- 3-methoxybenzyl)oxirane (68.8% yield) and 1-(3,4-dimethoxyphenyl)-3-ethoxypropan-2-ol (63.58% yield), were synthesized from methyl eugenol. This research found that the odour characteristic of 2-(4-ethyl-3-methoxybenzyl)oxirane[floral, fresh, slight lime and sweet]compounds, is clearly different from the odours of the 1-(3,4-dimethoxyphenyl)-3-ethoxypropan-2-ol [Glue-like, pungent, and Caramel-like]. It is evident from our observations that double bond substitution and functional alteration of the methyl eugenol modifies the perceived odour of methyl eugenol  derivative. Thus, structural modification overall led to an increase in odour potency. Keywords: Fragrance, Methly-Eugenol, Ether, Olfactory characteristic, Epoxidation.


1976 ◽  
Vol 12 (6) ◽  
pp. 714-714
Author(s):  
A. N. Krasovskii ◽  
P. M. Kochergin ◽  
A. B. Roman

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