1998
DOI: 10.1007/s007060050122
|View full text |Cite
|
Sign up to set email alerts
|

Das Chelierungsverhalten von Ce

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4

Citation Types

2
2
0

Year Published

2001
2001
2015
2015

Publication Types

Select...
4

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(4 citation statements)
references
References 0 publications
2
2
0
Order By: Relevance
“…Thus, the presence of different substituent influences the dissociation of compound due to their different effects [20]. Similar results have been reported by earlier studies on pyrimidine compounds where polarity of substituent affects basicity of compounds [21].…”
Section: Resultssupporting
confidence: 84%
“…Thus, the presence of different substituent influences the dissociation of compound due to their different effects [20]. Similar results have been reported by earlier studies on pyrimidine compounds where polarity of substituent affects basicity of compounds [21].…”
Section: Resultssupporting
confidence: 84%
“…The more acidic character of SB-2 is because of negative inductive effect of 4-CH 3 group. Thus, the presence of different substituent influences the dissociation of compound due to their different effects [20]. Similar results have been reported by earlier studies on pyrimidine compounds where polarity of substituent affects basicity of compounds [21].…”
Section: Resultssupporting
confidence: 84%
“…This is reasonable because the presence of p ‐OCH 3 and p ‐CH 3 groups (i.e., an electron‐donating effect) will enhance the electron density by their high positive inductive or mesomeric effect, whereby stronger chelation was formed and therefore the stability of the complexes. The low stability of p ‐NO 2 and p ‐Cl complexes can be attributed to the presence of NO 2 and Cl group in the p ‐position relative to the azo group, respectively. This is caused by the negative inductive effect of NO 2 and Cl group, which decreases its ability for chelation and therefore the stability of the complexes. For the ligands with the same metal ion at constant temperature, the stability of the chelates increases in the order p ‐OCH 3 > p ‐CH 3 > p ‐H > p ‐Cl > p ‐NO 2 40.…”
Section: Resultsmentioning
confidence: 99%
“…For the ligands with the same metal ion at constant temperature, the stability of the chelates increases in the order p ‐OCH 3 > p ‐CH 3 > p ‐H > p ‐Cl > p ‐NO 2 40.…”
Section: Resultsmentioning
confidence: 99%