1997
DOI: 10.1107/s0108270196014473
|View full text |Cite
|
Sign up to set email alerts
|

Two Schiff Base Ligands Derived from 1,2-Diaminoethane

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
6
0

Year Published

1997
1997
2011
2011

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 10 publications
(8 citation statements)
references
References 0 publications
2
6
0
Order By: Relevance
“…A concomitant decrease in the C-O distance is also noted [C5-O1 = 1.344 (3) Å versus C22-O3 = 1.316 (2) Å ]. The C7-N2 and C5-O1 distances are similar to the corresponding distances in 2,2 0 -(azinodimethylene)diphenol [1.285 (7) and 1.364 (8) Å ; Xu et al, 1994] and 2,2 0 -[(1,2ethanediyl)bis(nitrilopropylidyne)]bisphenol [1.295 (3) and 1.351 (3) Å ; Corden et al, 1997], which both exist in the phenol-imine tautomeric form. Likewise, the C24-N4 and C22-O3 bond lengths are similar to the corresponding distances in 2-{[tris(hydroxymethyl)methyl]aminomethylene}cyclohexa-3,5-dien-1(2H)-one [1.2952 18and 1.3025 (18) Å , respectively; Odabaşog lu et al, 2003] and 3-[(2-oxo-1naphthylidene)methylamino]benzoic acid [1.319 (3) and 1.290 (2) Å ; Pavlović & Sosa, 2000], which both show the keto-amine tautomeric form.…”
Section: Commentsupporting
confidence: 54%
“…A concomitant decrease in the C-O distance is also noted [C5-O1 = 1.344 (3) Å versus C22-O3 = 1.316 (2) Å ]. The C7-N2 and C5-O1 distances are similar to the corresponding distances in 2,2 0 -(azinodimethylene)diphenol [1.285 (7) and 1.364 (8) Å ; Xu et al, 1994] and 2,2 0 -[(1,2ethanediyl)bis(nitrilopropylidyne)]bisphenol [1.295 (3) and 1.351 (3) Å ; Corden et al, 1997], which both exist in the phenol-imine tautomeric form. Likewise, the C24-N4 and C22-O3 bond lengths are similar to the corresponding distances in 2-{[tris(hydroxymethyl)methyl]aminomethylene}cyclohexa-3,5-dien-1(2H)-one [1.2952 18and 1.3025 (18) Å , respectively; Odabaşog lu et al, 2003] and 3-[(2-oxo-1naphthylidene)methylamino]benzoic acid [1.319 (3) and 1.290 (2) Å ; Pavlović & Sosa, 2000], which both show the keto-amine tautomeric form.…”
Section: Commentsupporting
confidence: 54%
“…This phenomenon has been observed in similar systems 17 and was also confirmed by single crystal X-ray diffraction. 18 It can be concluded that the dissimilar two compartmental ligands 3 were prepared in satisfactory yields by a simple and convenient multistep method.…”
Section: Resultsmentioning
confidence: 99%
“…(H 2 B = BHPDE and X = NO 3 , Cl, or ½SO 4 ) The determined extraction constant, Kex, from equation 7as depicted in Figure 2 is 10 15.9 . The ligand behaves as a weak acid and in high pH media 13,14 formation of a chelate will probably be according to equation (8).…”
Section: Resultsmentioning
confidence: 99%
“…Bis(4-hydroxypent-2-ylidene)diaminoethane (BHPDE) has been synthesised and characterized via UV-Vis 1,2 , FTIR [3][4][5] and NMR 6,7 . Through these means it was established to exist in three tautomeric forms 8 . The coordination chemistry of BHPDE with divalent metal ions and the potentials of BHPDE as a photometric reagent and as extractant for Cu(II) and many other metal ions have been documented [9][10][11][12] .…”
Section: Introductionmentioning
confidence: 99%