The template effects exerted by guests 14 and 15 in the ring closure reaction of 3 have been quantitatively evaluated. The rate largely increases in the presence of the two templates. The results are compared with those relative to the ring closure reaction of 1 yielding cyclobis(paraquat-p-phenylene), 2. The comparison indicates that the formation of tetracationic aromatic cycles templated by aromatic donors benefits from the use of extended pi surfaces both in the acceptor and in the donor components.

Template effects in the formation of [2]pseudo-rotaxanes containing diazapyrenium units / Doddi, Giancarlo; Gianfranco, Ercolani; Mencarelli, Paolo; Giuseppe, Papa. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - STAMPA. - 72:4(2007), pp. 1503-1506. [10.1021/jo062115c]

Template effects in the formation of [2]pseudo-rotaxanes containing diazapyrenium units

DODDI, Giancarlo;MENCARELLI, Paolo;
2007

Abstract

The template effects exerted by guests 14 and 15 in the ring closure reaction of 3 have been quantitatively evaluated. The rate largely increases in the presence of the two templates. The results are compared with those relative to the ring closure reaction of 1 yielding cyclobis(paraquat-p-phenylene), 2. The comparison indicates that the formation of tetracationic aromatic cycles templated by aromatic donors benefits from the use of extended pi surfaces both in the acceptor and in the donor components.
2007
cations; cyclobis(paraquat-p-phenylene); interlocked molecules
01 Pubblicazione su rivista::01a Articolo in rivista
Template effects in the formation of [2]pseudo-rotaxanes containing diazapyrenium units / Doddi, Giancarlo; Gianfranco, Ercolani; Mencarelli, Paolo; Giuseppe, Papa. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - STAMPA. - 72:4(2007), pp. 1503-1506. [10.1021/jo062115c]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/235892
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