Carborane-functionalized polyaza aromatic ligands: Synthesis, crystal structure, and a copper(II) complex / Prokhorov AM,Kozhevnikov DN,Rusinov VL,Chupakhin ON,Glukhov IV,Antipin MY,Kazheva ON,Chekhlov AN,Dyachenko OA // ORGANOMETALLICS. - 2006. - V. 25, l. 12. - P. 2972-2977.

ISSN/EISSN:

0276-7333 / нет данных

Type:

Article

Abstract:

A consecutive aromatic nucleophilic substitutions of hydrogen in 1,2,4-triazine4-oxides and an aza Diels-Alder reaction is a versatile route to carborane-functionalized bi- and terpyridines and their 1,2,4-triazine analogues. The heterocycles facilitate deboronation of the substituted carboranes, and the carborane moiety has a significant influence on the coordination properties of the ligands as well.

Author keywords:

DIELS-ALDER REACTION; METALLOSUPRAMOLECULAR CHEMISTRY; 2,2'-BIPYRIDINE; DERIVATIVES; 1,2,4-TRIAZINES; STRATEGY

DOI:

10.1021/om051058v

Web of Science ID:

ISI:000237921000014

Соавторы в МНС:

Другие поля

Поле	Значение
Month	JUN 5
Publisher	AMER CHEMICAL SOC
Address	1155 16TH ST, NW, WASHINGTON, DC 20036 USA
Language	English
Keywords-Plus	DIELS-ALDER REACTION; METALLOSUPRAMOLECULAR CHEMISTRY; 2,2'-BIPYRIDINE; DERIVATIVES; 1,2,4-TRIAZINES; STRATEGY
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Inorganic \& Nuclear; Chemistry, Organic
Author-Email	dnk@htf.ustu.ru
ResearcherID-Numbers	Prokhorov, Anton/B-9789-2011
Number-of-Cited-References	28
Usage-Count-Since-2013	5
Journal-ISO	Organometallics
Doc-Delivery-Number	048AW