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Supramolecular engineering

Kahn O, Garcia Y, Letard JF, Mathoniere C (1999) Hysteresis and memory effect in supramolecular chemistry. In Veciana J (ed) Supramolecular engineering of synthetic metallic materials. Kluwer Academic, The Netherlands, p 127... [Pg.62]

Lohmeijer BGG, Schubert US (2002) Supramolecular engineering with macromolecules an alternative concept for block copolymers. Angew Chem Int Ed 41 3825-3829... [Pg.61]

The design of molecules, supermolecules and materials presenting NLO activity involves molecular and supramolecular engineering. At the molecular level, a high polarizability, leading to large quadratic ft and cubic y hyperpolarizability coeffi-... [Pg.100]

The directed manipulation of intermolecular interactions (hydrogen bonding, van der Waals forces, metal coordination) gives access to a supramolecular engineering of molecular assemblies and of polymers (see, for instance, [7.10-7.13, 7.44, 9.142, 9.157, 9.161-9.163]) through the design of instructed monomeric and polymeric species. It leads to the development of a supramolecular materials chemistry (see Section 9.8). [Pg.174]

The realization of efficient SHG materials involves performing supramolecular engineering on the compounds presenting pronounced NLO properties obtained by molecular engineering. This may be achieved by introducing the molecules into organized phases such as molecular films, liquid crystals or solid state structures, by suitable derivatization or mixing with host substances. [Pg.441]

Kuhn, Hans, A Model of the Origin of Life and Perspectives in Supramolecular Engineering, 1, 247. [Pg.224]

Fig. 1.10 A curricular structure discussed during the Touchstones of Modem Polymer Processing workshop, where a novel discipline called Molecular and Supramolecular Engineering and Science, becomes the initial, common core of macromolecular, chemical molecular, and Biomacromolecular engineering. Fig. 1.10 A curricular structure discussed during the Touchstones of Modem Polymer Processing workshop, where a novel discipline called Molecular and Supramolecular Engineering and Science, becomes the initial, common core of macromolecular, chemical molecular, and Biomacromolecular engineering.
Veciana J, Rovira C, Amabilino DB (1999) Supramolecular Engineering of Synthetic Metallic Materials. NATO ASI Series C,518. Kluwer Academic, Dordrecht... [Pg.295]

Bernstein, J. (1999). Structural and crystallographic aspects of supramolecular engineering. In Supramolecular engineering of synthetic metallic materials (ed. J. Veciana, C. Rovira and D. B. Amabilino), pp. 23-40. Kluwer, Dordrecht, The Netherlands. [194f, 200f]... [Pg.314]

Simon, J., and Pierre Bassoul. Design of Molecular Materials Supramolecular Engineering. New York Wiley, 2000. [Pg.306]

The hydrogen carbonate XHCO3 family with X = Na, K, Rb, Cs is interesting in the context of both supramolecular engineering and HB studies, because it gives a series of ionic compounds with hydrogen-bonded dimers... [Pg.149]

Ram M. K. (ed.). The Supramolecular Engineering of Conducting Materials (Trivandrum, Kerela, India Transworld Research Network, 2005). [Pg.66]

Wurthner, F., Kaiser, Th.E., Saha-Moller, Ch.R. (2011). J-Aggregates From Serendipitous Discovery to Supramolecular Engineering of Functional Dye Materials. Angew. Chem, Int, Ed, Vol.50. pp. 3376 - 3410. [Pg.356]

The efficacy of this supramolecular engineering strategy was first demonstrated for heterocyclic rod-coil copolymers, with poly(p-phenylenebenzobisthiazole) (PBZT) and derivatives used as the rod-like segments(7Q). The wavelength of absorption and emission of rod-coil copolymers... [Pg.476]

Supramolecular engineering of perylene bisimide assembHes based on complementary multiple hydrogen bonding interactions 13AJO 708. [Pg.291]

J. Roncali, P. Frere, P. Blanchard, R. de Bettignies, M. Turbiez, S. Roquet, P. Leriche and Y. Nicolas, Molecular and supramolecular engineering of jr-conjugated systems for photovoltaic conversion. Thin Solid Films, 511-512, 567-575 (2006). [Pg.290]

Fechtenkotter A, Tchebotareva N, Watson MD, Mullen K (2001) Discotic liquid crystalline hexabenzocoronenes carrying chiral and racemic branched alkyl chains supramolecular engineering and improved synthetic methods. Tetrahedron 57 3769-3783... [Pg.247]

Extension of this self-assembly approach to supramolecular engineering has led to an alternate motif for noncovalent cross-linking, a series of bisthymines that are complementary to the diamidopyridine side chains of polymer 6 (33). Upon combination in non-polar media thermally reversible, micrometer scale spherical aggregates were formed (Figs. 13b and 13c). [Pg.4908]


See other pages where Supramolecular engineering is mentioned: [Pg.383]    [Pg.138]    [Pg.193]    [Pg.194]    [Pg.436]    [Pg.437]    [Pg.441]    [Pg.21]    [Pg.760]    [Pg.280]    [Pg.357]    [Pg.490]    [Pg.323]    [Pg.2]    [Pg.254]    [Pg.370]   
See also in sourсe #XX -- [ Pg.174 , Pg.193 ]




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