http://www.cnr.it/ontology/cnr/individuo/prodotto/ID169595
Structure-Property Relationships in Densely Grafted À-Stacked Polymers (Articolo in rivista)
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- Structure-Property Relationships in Densely Grafted À-Stacked Polymers (Articolo in rivista) (literal)
- Anno
- 2010-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/pola.24016 (literal)
- Alternative label
Cappelli A., Paolino M., Anzini P., Giuliani G., Valenti S., Aggravi M., Donati A., Mendichi R., Zetta L., Boccia A. C., Bertini F., Samperi F., Battiato S., Paccagnini S., Vomero S. (2010)
Structure-Property Relationships in Densely Grafted À-Stacked Polymers
in Journal of polymer science. Part A, Polymer chemistry
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Cappelli A., Paolino M., Anzini P., Giuliani G., Valenti S., Aggravi M., Donati A., Mendichi R., Zetta L., Boccia A. C., Bertini F., Samperi F., Battiato S., Paccagnini S., Vomero S. (literal)
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- http://onlinelibrary.wiley.com/doi/10.1002/pola.24016/pdf (literal)
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Mendichi R., Zetta L., Boccia A. C., Bertini F.; Istituto per lo Studio delle Macromolecole (CNR), Milano, Italy
Cappelli A., Paolino M., Anzini P., Giuliani G., Valenti S., Aggravi M., Donati A., Paccagnini S., Vomero S.; Università di Siena, Siena, Italy
Samperi F., Battiato S.; Istituto di Chimica e Tecnologia dei Polimeri (CNR), Catania, Italy. (literal)
- Titolo
- Structure-Property Relationships in Densely Grafted À-Stacked Polymers (literal)
- Abstract
- Three methyl end-capped oligo(ethylene glycol) (MOEG) ethers (1b-d) and a methoxyderivative (1a) of benzofulvene monomer BF3k were synthesized and induced to polymerize spontaneously by solvent removal to obtain soluble À-stacked polymers bearing densely grafted MOEG side chains (poly-1b-d) and model polymer poly-1a. The physicochemical features (e.g., solubility, NMR, MALDI-TOF, and absorption/emission spectra, as well as MWD, conformation plot, and thermal properties) of the synthesized polymers were compared in a structure-property relationship study. This approach afforded the following evidence. The structure of poly-1a-d is very similar to that of BF3k, suggesting that the polymerization mechanism is not affected by the presence of the electron-rich methoxy group or bulkier MOEG side chains. However, the latter appear to be capable of affecting the conformational behavior of the polymer backbone. The solubility of poly-1a-d depends on the number of the oligo (ethylene glycol) monomeric units. In particular, poly-1d, featuring a long MOEGside chain (n = 9), shows an amphiphilic character and is soluble in a number of organic solvents, whereas it interacts with water to give isolated macromolecules in equilibrium with nanosized water-soluble aggregates. (literal)
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