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Interfaces Involving Biomolecules and Inorganic Materials: a Solid State NMR Approach

Published online by Cambridge University Press:  01 February 2011

Christian Bonhomme
Affiliation:
[email protected], Universite P et M Curie, Laboratoire chimie de la matière condensée, 4 place Jussieu, Paris, N/A, France, 33 1 44 27 41 35, 33 1 44 27 47 69
Geoffrey Hartmeyer
Affiliation:
[email protected], Universite P et M Curie, Laboratoire chimie de la matière condensée, 4 place Jussieu, Paris, N/A, France
Florence Babonneau
Affiliation:
[email protected], Universite P et M Curie, Laboratoire chimie de la matière condensée, 4 place Jussieu, Paris, N/A, France
Michel Wong Chi Man
Affiliation:
[email protected], ENSCM, Heterochimie moleculaire et supramoleculaire, Montpellier, 34296, France
Guilhem Arrachart
Affiliation:
[email protected], ENSCM, Heterochimie moleculaire et supramoleculaire, Montpellier, 34296, France
Carole Carcel
Affiliation:
[email protected], ENSCM, Heterochimie moleculaire et supramoleculaire, Montpellier, 34296, France
Joel Moreau
Affiliation:
[email protected], ENSCM, Heterochimie moleculaire et supramoleculaire, Montpellier, 34296, France
Bruno Alonso
Affiliation:
[email protected], ENSCM, UMR 5223 MACS, Montpellier, 34296, France
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Abstract

Materials based on ureidopyrimidinone (UPY) dimers and Adenine (A) / Thymine (T) derivatives were synthesized and characterized by advanced solid state NMR (Nuclear Magnetic Resonance) techniques. Silylated UPY molecules were used as model compounds, leading to structured organic-inorganic materials after hydrolysis and condensation processes (sol-gel reactions). High resolution 1H solid state NMR has been extensively used for the in-depth description of the H-bond networks, including very fast MAS (Magic Angle Spinning) experiments at very high field and DQ (double quantum) recoupling experiments. The chemical nature of the organic-inorganic interface has been illuminated by such techniques. In, particular, it has been demonstrated that H-bond networks were preserved during sol-gel reactions and were comparable to those observed in the UPY crystalline precursors.

Type
Research Article
Copyright
Copyright © Materials Research Society 2007

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References

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