http://www.cnr.it/ontology/cnr/individuo/prodotto/ID33166
Template Effect of Tetrathiafulvalene in the Formation of Cyclobis(Paraquat-p-Phenylene) (Articolo in rivista)
- Type
- Label
- Template Effect of Tetrathiafulvalene in the Formation of Cyclobis(Paraquat-p-Phenylene) (Articolo in rivista) (literal)
- Anno
- 2005-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/jo050263h (literal)
- Alternative label
Doddi G., Ercolani G., Mencarelli P., Piermattei A. (2005)
Template Effect of Tetrathiafulvalene in the Formation of Cyclobis(Paraquat-p-Phenylene)
in Journal of organic chemistry
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Doddi G., Ercolani G., Mencarelli P., Piermattei A. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Dipartimento di Chimica e CNR-IMC, Universita` di Roma La Sapienza,
Dipartimento di Scienze e Tecnologie Chimiche, Universita` di Roma Tor Vergata (literal)
- Titolo
- Template Effect of Tetrathiafulvalene in the Formation of Cyclobis(Paraquat-p-Phenylene) (literal)
- Abstract
- The template effect exerted by tetrathiafulvalene (TTF) in the ring-closure reaction of the trication 5(3+) yielding cyclobis(paraquat-p-phenylene) has been quantitatively evaluated in acetonitrile at 62 degrees C with UV-vis spectrophotometry. The rate of ring closure of the trication 5(3+) largely increases in the presence of the template (a maximum increase of ca. 80 times at [TTF] approximate to 0.14 M). The results are compared with those of other aromatic templates, 2 and 3, that were provided with polyethereal sidearms and indicate that the template ability of tetrathiafulvalene is comparable or better than that of the others. (literal)
- Prodotto di
- Autore CNR
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