Publikace detail

A comparative study of the structure and bonding in heavier pnictinidene complexes [(ArE) M(CO)(n)] (E = As, Sb and Bi; M = Cr, Mo, Wand Fe)

Rok: 2017

Druh publikace: článek v odborném periodiku

Název zdroje: Dalton Transactions

Název nakladatele: Royal Society of Chemistry

Místo vydání: Cambridge

Strana od-do: 3556-3568

Tituly:

Jazyk	Název	Abstrakt	Klíčová slova
cze	Studie struktury a vazebné situace v pniktinidýnových komplexech [(ArE) M(CO)(n)] (E = As, Sb and Bi; M = Cr, Mo, Wand Fe)	Byla studována struktura a vazebné situace v pniktinidýnových komplexech [(ArE) M(CO)(n)] (E = As, Sb and Bi; M = Cr, Mo, W a Fe)
eng	A comparative study of the structure and bonding in heavier pnictinidene complexes [(ArE) M(CO)(n)] (E = As, Sb and Bi; M = Cr, Mo, Wand Fe)	N, C, N-Chelated pnictinidenes ArE [where E = As (1), Sb (2) or Bi (3); Ar = C6H3-2,6-(CHvNt-Bu)(2)] were used as ligands for the coordination of transition metal carbonyls. Thus, the reaction of 1-3 with [M(CO)(5)THF] (where M = Cr, W) or [Mo(CO)(5)(Me3N)] gave complexes [(ArE)M(CO)(5)] [where E = As and M = Cr (1a), Mo (1b), W (1c); E = Sb and M = Cr (2a), Mo (2b), W (2c); E = Bi and M = Cr (3a), Mo (3b), W (3c)]. Analogously, the treatment of 1-3 with [Fe-2(CO)(9)] resulted in the formation of the complexes [(ArE)Fe(CO)(4)] [where E = As (1d), Sb (2d) or Bi (3d)]. All compounds were characterized by H-1 and C-13 NMR spectroscopy, Raman, IR and UV-Vis spectroscopy. The molecular structures of the majority of the compounds (except 1b and 1c) were also determined by the single-crystal X-ray diffraction analysis. Furthermore, the structure and bonding of the title compounds have also been thoroughly investigated using a computational approach.	transition-metal-complexes; ray crystal-structures; main-group compounds; coordination chemistry; carbene-phosphinidene; covalent radii; phosphanylidene-phosphorane; carbonyl-complexes; infrared-spectra; dative bonds

Vyhledávání

Přihlášení pro studenty

Přihlášení pro zaměstnance

Publikace detail

Katedry

Ústavy a pracoviště

Jak nás najdete?

Služby

Často hledáte