Molecular recognition of aromatic carboxylic acids by hydroxypropyl-γ-cyclodextrin: experimental and theoretical evidence

RSC Advances ◽  
2016 ◽  
Vol 6 (55) ◽  
pp. 49567-49577 ◽  
Author(s):  
Irina Terekhova ◽  
Roman Kumeev ◽  
Gennady Alper ◽  
Sandipan Chakraborty ◽  
Horacio Pérez-Sánchez ◽  
...  

Inclusion complex formation of hydroxypropyl-γ-cyclodextrin with benzoic, nicotinic and isomeric aminobenzoic acids in water was studied by calorimetry, 1H NMR, densimetry and molecular modeling.

Author(s):  
Narayanasamy Rajendiran ◽  
J. Thulasidhasan ◽  
M. Jude Jenita

The inclusion complexation of 2-aminobenzoic acid (2ABA), 3-aminobenzoic acid (3ABA), and 4-aminobenzoic acid (4ABA) with α-cyclodextrin (α-CD), β-cyclodextrin (β-CD), hydroxypropyl-α-cyclodextrin (HP-α-CD) and hydroxypropyl-β-cyclodextrin (HP-β-CD) were studied in buffer solutions of differentpHs (pH~1 andpH~7) and it was carried out using UV-Visible, steady-state and time-resolved fluorescence. Dual fluorescence was observed for all the compounds in aqueous and CD medium. All the ABAs forms 1:1 inclusion complex at pH ~ 1 solution and mixture of 1:1 and 1:2 inclusion complex at pH ~7. With CDs, dual luminescence appeared at pH ~ 1 indicates, both NH3+and COOH groups are present in the interior of the CDs cavities. FT-IR,1H NMR, results suggest ABAs formed a stable inclusion complex with the CDs.


2000 ◽  
Vol 69 (2) ◽  
pp. 129-133 ◽  
Author(s):  
Narpinder Singh ◽  
Kulwinder Kaur ◽  
Hardeep Singh ◽  
Harmeet Singh

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