The structure of 1,1′-(2,6-pyridindiyl)bis[6,7-dihydro-4-(4-methoxyphenyl)-5H-cyclopenta[c]pyridine

Authors

  • A. V. Rybakova South Ural State University
  • S. E. Vatolina Ural Federal University
  • A. P. Krinochkin Ural Federal University; I.Ya. Postovsky Insititute of Organic Synthesis of UB of the RAS
  • V. S. Gaviko Уральский федеральный университет;
  • O. V. Shabunina Sirius University of Science and Technology
  • Yu. М. Sayfutdinova Ural Federal University
  • А. S. Мarkina Ural Federal University
  • А. S. Alekseeva Ural Federal University
  • D. S. Kopchuk Ural Federal University; I.Ya. Postovsky; Insititute of Organic Synthesis of UB of the RAS
  • G. V. Zyryanov Ural Federal University; I.Ya. Postovsky; Insititute of Organic Synthesis of UB of the RAS

Keywords:

2, 2', 6', 2''-terpyridines, Bodger reaction, X-ray crystallography

Abstract

1,1'-(2,6-Pyridinediyl)bis[6,7-dihydro-4-(4-methoxyphenyl)-5H-cyclopenta[c]pyridine was obtained in good yield (52%) by reacting 3,3'-(2,6-pyridinediyl)bis[6-(4-methoxyphenyl)-1,2,4-triazine] with 1-morpholincyclopene during its solvent-free fusion at 200 °C, i.e., the PASE approach was implemented in contrast to the previously proposed boiling in 1,4-dioxane in the literature. The structure of the obtained compound was studied in detail using X-ray structure analysis of its single crystal, and a comparison was made with information previously described in the literature (in particular, the bond lengths between atoms and the valence angles, as well as the mutual arrangement of aromatic fragments). The features of the supramolecular structure of the obtained compound that had not been described previously were characterized, including the arrangement of two monomers stacked head-to-head, which ensured the minimal distance between adjacent structures.

Author Biographies

A. V. Rybakova, South Ural State University

кандидат химических наук, доцент, доцент кафедры теоретической и прикладной химии

S. E. Vatolina, Ural Federal University

лаборант-исследователь Лаборатории перспективных материалов, зеленых методов и биотехноло-гии НОиИЦ ХФТ ХТИ

A. P. Krinochkin, Ural Federal University; I.Ya. Postovsky Insititute of Organic Synthesis of UB of the RAS

кандидат химических наук, младший научный сотрудник Технологической лаборатории; научный сотрудник кафедры органической и биомолекулярной химии ХТИ

V. S. Gaviko, Уральский федеральный университет;

Ural Federal University; M.N. Mikheev lnstitute of Metal Physics of UB of the RAS

O. V. Shabunina, Sirius University of Science and Technology

кандидат химических наук, доцент Научного центра трансляционной медицины

Yu. М. Sayfutdinova, Ural Federal University

младший научный сотрудник лаборатории перспективных материалов, зеленых методов и биотехнологий НОиИЦ ХФТ ХТИ

А. S. Мarkina, Ural Federal University

лаборант-исследователь лаборатории перспективных материалов, зеленых методов и биотехнологий НОиИЦ ХФТ ХТИ

А. S. Alekseeva, Ural Federal University

лаборант-исследователь лаборатории перспективных материалов, зеленых методов и биотехнологий НОиИЦ ХФТ ХТИ

D. S. Kopchuk, Ural Federal University; I.Ya. Postovsky; Insititute of Organic Synthesis of UB of the RAS

доктор химических наук, старший научный сотрудник Лаборатории координационных соединений; младший научный сотрудник кафедры органической и биомолекулярной химии ХТИ

G. V. Zyryanov, Ural Federal University; I.Ya. Postovsky; Insititute of Organic Synthesis of UB of the RAS

доктор химических наук, профессор РАН, ведущий научный сотрудник лаборатории координационных соединений; профессор кафедры органической и биомолекулярной химии ХТИ

Published

2026-03-15