Preparation and Spectroscopic Study of Different Stoichiometric Solid Supramolecular Inclusion Complexes of -Cyclodextrin with Short Chain Aliphatic Amines

2008 ◽  
Vol 21 (2) ◽  
pp. 174-180 ◽  
Author(s):  
Le-xin Song ◽  
Chuan-feng Teng ◽  
Hai-ming Wang ◽  
Lei Bai
Keyword(s):  
Spectroscopic Study ◽  
Inclusion Complexes ◽  
Aliphatic Amines ◽  
Short Chain

scholarly journals Computer simulation and spectroscopic study of inclusion complexes of cyclodextrins with luminescent porphyrins

2010 ◽  
Vol 249 ◽  
pp. 012037 ◽  
Author(s):  
George R S Andrade ◽  
Thiago dos S Rezende ◽  
Ledjane S Barreto ◽  
Luis E Almeida ◽  
Nivan B da Costa ◽  
...  
Keyword(s):  
Computer Simulation ◽  
Spectroscopic Study ◽  
Inclusion Complexes

Short-chain aliphatic amines in human urine: a mathematical examination of metabolic interrelationships

Metabolism ◽  
2007 ◽  
Vol 56 (1) ◽  
pp. 19-23 ◽  
Author(s):  
Stephen C. Mitchell ◽  
Mary E. Bollard ◽  
AiQin Zhang
Keyword(s):  
Human Urine ◽  
Aliphatic Amines ◽  
Short Chain

scholarly journals NMR spectroscopic study of inclusion complexes of cetirizine dihydrochloride and β-cyclodextrin in solution

2007 ◽  
Vol 21 (3) ◽  
pp. 177-182 ◽  
Author(s):  
Syed Mashhood Ali ◽  
Santosh Kumar Upadhyay ◽  
Arti Maheshwari
Keyword(s):  
Aqueous Solution ◽  
Chemical Shift ◽  
Spectroscopic Study ◽  
Inclusion Complexes ◽  
Binding Constant ◽  
Spectroscopic Studies ◽  
Chemical Shift Change ◽  
Nmr Chemical Shift ◽  
H Nmr ◽  
Shift Change

Cetirizine dihydrochloride (CTZ), an antihistamine, forms two 1:1 inclusion complexes with β-cyclodextrin (β-CD) in aqueous solution as confirmed by detailed1H NMR, COSY and ROESY spectroscopic studies. The stoichiometry and overall binding constant of the complexes were determined by the treatment of1H NMR chemical shift change (Δδ) data. Most of the CTZ protons exhibited splitting in the presence of β-CD.

Spectroscopic study on the inclusion complexes of β-cyclodextrin with selected metabolites of catecholamines

2017 ◽  
Vol 1127 ◽  
pp. 532-538 ◽  
Author(s):  
Anna Korytkowska-Wałach ◽  
Beata Dubrawska ◽  
Monika Śmiga-Matuszowicz ◽  
Tadeusz Bieg
Keyword(s):  
Spectroscopic Study ◽  
Inclusion Complexes

The anesthetic potency of n-alcohols. A model spectroscopic study in inverted micelles

1986 ◽  
Vol 64 (3) ◽  
pp. 633-634 ◽  
Author(s):  
Pierre Ménassa ◽  
Thérèse Lussier ◽  
Camille Sandorfy
Keyword(s):  
Spectroscopic Study ◽  
Association Constants ◽  
Point Of View ◽  
Short Chain ◽  
Polar Groups ◽  
Anesthetic Potency ◽  
Long Chain

A relation has been found between the anesthetic potency of n-alcohols (n = 1, 3, 6, 7, 9, 11, 14, and 16) and their association constants with polar groups in inverted micelles. From this point of view, cholesterol and 7-dehydrocholesterol behave like short-chain n-alcohols while cholestanol behaves like a long-chain n-alcohol.

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