Structural Properties of Chemically Modified Cyclodextrins: The Crystal Structure of an Inclusion Complex between Adamantanol and per-2,6-0-Methyl-β-Cyclodextrin

1982 ◽  
pp. 151-161 ◽  
Author(s):  
John J. Stezowski ◽  
Mátyás Czugler ◽  
Emil Eckle
Keyword(s):  
Crystal Structure ◽  
Inclusion Complex ◽  
Structural Properties ◽  
Chemically Modified ◽  
Modified Cyclodextrins

Crystal structure of an inclusion complex between chiral monoaza-15-crown-5 and S(–)-1-phenyl-ethyl ammonium percholorate

2003 ◽  
Vol 218 (5) ◽  
Author(s):  
Süheyla Özbey ◽  
F. B. Kaynak ◽  
M. Toğrul ◽  
N. Demirel ◽  
H. Hoşgören
Keyword(s):  
Crystal Structure ◽  
Inclusion Complex ◽  
Single Crystal ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
New Type

AbstractA new type of inclusion complex, S(–)-1 phenyl ethyl ammonium percholorate complex of R-(–)-2-ethyl - N - benzyl - 4, 7, 10, 13 - tetraoxa -1- azacyclopentadecane, has been prepared and studied by NMR, IR and single crystal X-ray diffraction techniques. The compound crystallizes in space group

ChemInform Abstract: Formation and Crystal Structure of an Unexpected Inclusion Complex of a Metal-Free Phthalocyanine and Oxalic Acid.

ChemInform ◽  
2010 ◽  
Vol 33 (29) ◽  
pp. no-no
Author(s):  
Wei Liu ◽  
Chi-Hang Lee ◽  
Hung-Wing Li ◽  
Chi-Keung Lam ◽  
Jinzhi Wang ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Oxalic Acid ◽  
Inclusion Complex ◽  
Metal Free

Thermodynamic and structural properties of palladium(II) polynuclear complexes of azamacrocycles. Crystal structure of the [Pd2([24]aneN8)] (ClO4)4 complex

1993 ◽  
Vol 32 (7) ◽  
pp. 1204-1208 ◽  
Author(s):  
Andrea Bencini ◽  
Antonio Bianchi ◽  
Paolo Dapporto ◽  
Enrique Garcia-Espana ◽  
Piero Paoletti ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Structural Properties ◽  
Polynuclear Complexes

scholarly journals Guest-Host Inclusion Complex Formation of 2-, 3-, and 4-Aminobenzoic Acids with Native and Modified Cyclodextrins

2016 ◽  
Vol 69 ◽  
pp. 10-21 ◽  
Author(s):  
Narayanasamy Rajendiran ◽  
J. Thulasidhasan ◽  
M. Jude Jenita
Keyword(s):  
Inclusion Complex ◽  
Inclusion Complexation ◽  
Aminobenzoic Acid ◽  
Time Resolved ◽  
H Nmr ◽  
Buffer Solutions ◽  
Aminobenzoic Acids ◽  
Modified Cyclodextrins ◽  
Ft Ir ◽  
Uv Visible

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.

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