Designing fluorous domains. Synthesis of a series of pyridinium salts bearing a perfluoroalkylated azole moiety

Ivana Pibiri; Andrea Pace; Silvestre Buscemi; Nicolo' Vivona; Luciana Malpezzi

Designing fluorous domains. Synthesis of a series of pyridinium salts bearing a perfluoroalkylated azole moiety

Ivana Pibiri, Andrea Pace, Silvestre Buscemi, Nicolo' Vivona, Luciana Malpezzi

Scienze e Tecnologie Biologiche Chimiche e Farmaceutiche

Risultato della ricerca: Article › peer review

17 Citazioni (Scopus)

Abstract

The synthesis of a series of N-methylpyridinium salts bearing a perfluoroalkylated 1,2,4-oxadiazole or 1,2,4-triazole moiety is reported. X-Ray structures of representative perfluoroalkyl-triazolylpyridine (15) and methylpyridinium iodide salt (5a) are reported. Their crystal packing clearly shows segregation between the aromatic and parallel double layer fluorinated regions.

Lingua originale	English
pagine (da-a)	307-321
Numero di pagine	15
Rivista	Heterocycles
Volume	68
Stato di pubblicazione	Published - 2006

All Science Journal Classification (ASJC) codes

Analytical Chemistry
Pharmacology
Organic Chemistry

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title = "Designing fluorous domains. Synthesis of a series of pyridinium salts bearing a perfluoroalkylated azole moiety",

abstract = "The synthesis of a series of N-methylpyridinium salts bearing a perfluoroalkylated 1,2,4-oxadiazole or 1,2,4-triazole moiety is reported. X-Ray structures of representative perfluoroalkyl-triazolylpyridine (15) and methylpyridinium iodide salt (5a) are reported. Their crystal packing clearly shows segregation between the aromatic and parallel double layer fluorinated regions.",

author = "Ivana Pibiri and Andrea Pace and Silvestre Buscemi and Nicolo' Vivona and Luciana Malpezzi",

year = "2006",

language = "English",

volume = "68",

pages = "307--321",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

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T1 - Designing fluorous domains. Synthesis of a series of pyridinium salts bearing a perfluoroalkylated azole moiety

AU - Pibiri, Ivana

AU - Pace, Andrea

AU - Buscemi, Silvestre

AU - Vivona, Nicolo'

AU - Malpezzi, Luciana

PY - 2006

Y1 - 2006

N2 - The synthesis of a series of N-methylpyridinium salts bearing a perfluoroalkylated 1,2,4-oxadiazole or 1,2,4-triazole moiety is reported. X-Ray structures of representative perfluoroalkyl-triazolylpyridine (15) and methylpyridinium iodide salt (5a) are reported. Their crystal packing clearly shows segregation between the aromatic and parallel double layer fluorinated regions.

AB - The synthesis of a series of N-methylpyridinium salts bearing a perfluoroalkylated 1,2,4-oxadiazole or 1,2,4-triazole moiety is reported. X-Ray structures of representative perfluoroalkyl-triazolylpyridine (15) and methylpyridinium iodide salt (5a) are reported. Their crystal packing clearly shows segregation between the aromatic and parallel double layer fluorinated regions.

UR - http://hdl.handle.net/10447/25536

M3 - Article

VL - 68

SP - 307

EP - 321

JO - Heterocycles

JF - Heterocycles

SN - 0385-5414

ER -