trans-Dimethanolbis(quinoline-8-carboxylato-κ²N,O)cobalt(II)

Abstract

Key indicatorsSingle-crystal X-ray study T = 293 K Mean (C-C) = 0.004 Å R factor = 0.036 wR factor = 0.089 Data-to-parameter ratio = 12.8For details of how these key indicators were automatically derived from the article, see

Diaquabis(3,7-dichloroquinoline-8-carboxylato)zinc(II) monohydrate

“…Quinolinecarboxylate derivatives and their complexes have attracted considerable interest, because of their interesting high germicidal, antitumoral and pharmacological properties (Adnan et al, 2003;Lumme et al, 1984). Although some transition metal complexes of quinolinecarboxylate ligands have been reported (Che et al, 2005;Chen et al, 2001;Yang et al, 2005), the crystal structures of the 3,7-Dichloro-8-quinolinecarboxylate and its complexes are limited in number, the only two examples are [M(C 10 H 4 Cl 2 NO 2 ) 2 ] n (M = Ni, Co) (Li et al, 2008;Zhang et al, 2007). we report herein on the…”

Ethyl 3,7-dichloroquinoline-8-carboxylate

“…For the usual preparative route, see: Yang et al (2002). For related complexes, see: An et al (2008); Che et al (2005); Guo (2008); Li et al (2008); Turel et al (2004); Zhang et al (2007). For 3,7-dichloroquinoline-8-carboxylic acid derivatives, see: Liang et al (2006);…”

“…Usually, it was prepared via Skraup cyclization from 2-methyl-3-chloroaniline, followed by chlorination and oxidation (Yang et al, 2002). Furthermore, quinolinecarboxylates can chelate to metal atoms, forming the complexes, such as trans-Dimethanolbis(quinoline-8- (Che et al,2005) et al, 2008). More recently, we also have reported a Zinc-quinclorac complex (An et al, 2008) and quinclorac (Guo, 2008).…”