2000
DOI: 10.1002/1099-0690(200004)2000:7<1235::aid-ejoc1235>3.0.co;2-8
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Nucleophilic Additions of Sodium Alkoxides to 4,4-Dichloro-1,1-diphenyl-2-azabuta-1,3-diene

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Cited by 10 publications
(6 citation statements)
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“…Chemistry 2024, 6 67 The values of the four-coordinate geometry index τ4 [45] are 0.83 and 0.71, and those The values of the four-coordinate geometry index τ4 [45] are 0.83 and 0.71, and those of τ4′ [46] are equal to 0.81 and 0.66 for 1 and 2, respectively. For the Cd complex 1, these (a) Iodine atom on the major site of occupancy equal to 0.93(1) (see experimental section).…”
Section: Molecular Structuresmentioning
confidence: 99%
See 1 more Smart Citation
“…Chemistry 2024, 6 67 The values of the four-coordinate geometry index τ4 [45] are 0.83 and 0.71, and those The values of the four-coordinate geometry index τ4 [45] are 0.83 and 0.71, and those of τ4′ [46] are equal to 0.81 and 0.66 for 1 and 2, respectively. For the Cd complex 1, these (a) Iodine atom on the major site of occupancy equal to 0.93(1) (see experimental section).…”
Section: Molecular Structuresmentioning
confidence: 99%
“…In contrast to the plethora of 1,4-diazabutadien (α-diimine) complexes [1-3], 2-azabutadienes R 2 C=C(H)-N=CR ′ 2 (R, R ′ = Hal, alkyl, aryl) featuring a π-conjugated C=C(H)-N=C array are far less common as ligands in coordination chemistry [4]. We have developed an access to π-conjugated Cl 2 C=C(H)-N=CAr 2 via 1,3-dipolar cycloaddition and demonstrated that the chlorine atoms therein can be readily substituted with alcoholates, amides and thiolates [5][6][7][8][9]. The latter ditopic thioether-functionalized 2-azabutadienes (RS) 2 C=C(H)-N=CAr 2 in turn represent versatile ligands in coordination chemistry, since they dispose of both a harder imine-type N-donor site and a soft S-thioether site, allowing a chelating coordination on various transition metal centers.…”
Section: Introductionmentioning
confidence: 99%
“…In the context of our interest in developing novel -conjugated dithioether compounds as ligands for coordination chemistry and further organic transformations, we have reported on the synthesis and crystal structure of 4,4-dichloro-1,1-diphenyl-2-azabuta-1,3-diene [Ph 2 C N-C(H) CCl 2 ] and its conversion to [Ph 2 C N-C(H) C(SR) 2 ] and [Ph 2 C N-C(H) C(OPh) 2 ] by reaction with thiolates NaSR or NaOPh, respectively (Jacquot et al, 1999(Jacquot et al, , 2000Jacquot-Rousseau et al, 2006;Kinghat et al, 2016). Several crystal structures of these molecules/ligands and their derived transition metal complexes reveal that despite the overall planarity of the -conjugated chain, one aryl group of the -N CPh 2 imine segment is tilted with respect to the azabutadienic array (Jacquot et al, 1999;Knorr et al, 2003;Kinghat et al, 2008).…”
Section: Chemical Contextmentioning
confidence: 99%
“…Some related structures of alkoxo- (Jacquot et al, 2000), cyano- (Jacquot-Rousseau et al, 2002) and i PrS-substituted (Jacquot-Rousseau et al, 2005) 4,4-dichloro-1,1-diphenyl-2azabuta-1,3-dienes (Jacquot et al, 1999) have been reported. For related literature, see: Tanimoto et al (1976); Truce & Boudakian (1956).…”
Section: Related Literaturementioning
confidence: 99%