1993
DOI: 10.1007/bf00817298
|View full text |Cite
|
Sign up to set email alerts
|

Structural studies on 3-acetyl-1,5-diaryl and 3-cyano-1,5-diaryl formazan chelates with cerium(III), thorium(IV) and uranium(VI)

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
3
0

Year Published

2003
2003
2021
2021

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 10 publications
(4 citation statements)
references
References 8 publications
1
3
0
Order By: Relevance
“…This proves that OH group takes part in the formation of C-O-M bond. These results are in good accordance with the literature [5,8,11,26] and confirm the structure given in Scheme1. Some, other aromatic C-H, SO2, S-O stretching peaks and -C-O-M vibration band in the compounds were observed in their expected regions.…”
Section: Ir Spectrasupporting
confidence: 92%
See 2 more Smart Citations
“…This proves that OH group takes part in the formation of C-O-M bond. These results are in good accordance with the literature [5,8,11,26] and confirm the structure given in Scheme1. Some, other aromatic C-H, SO2, S-O stretching peaks and -C-O-M vibration band in the compounds were observed in their expected regions.…”
Section: Ir Spectrasupporting
confidence: 92%
“…The fastness values were determined according to the International Standards; the specific tests used were ISO 105 C06/C1S (washing fastness), ISO 105X12 (treatment fastness) and ISO 105 B02 (light fastness). The light fastness tests were assessed according to the international blue scale (1)(2)(3)(4)(5)(6)(7)(8), the treatment and washing fastness tests were assessed according to the international grey scale (1-5), with scales 8 and 5, respectively, to find the best rank, while scale 1 was the most inferior. All fastness values of dyes were depicted in the Table 5.…”
Section: Fastness Testsmentioning
confidence: 99%
See 1 more Smart Citation
“…Formazans have the general formula R 1 –NH–NCR 2 –NN–R 3 , bearing both a hydrazone and an azo group and commonly exhibiting intense colors. They have synthetic applications, such as in the production of open-shell verdazyl compounds or as versatile formazanate ligands in organometallic complexes. Formazans can be obtained by the reductive reaction of the corresponding, usually colorless, tetrazolium salt, which is accompanied by a distinct color change. This chromogenic reaction has numerous applications, for example, using the enzymatic reduction of tetrazolium salts to formazans in biological assays to indicate cellular respiration and cell growth, in agriculture to examine the germinability of seeds, , in chromatographic sugar determination, and in medicine, especially in cancer research, or most recently the oxidation of amino acids by excited tetrazolium salts. , …”
Section: Introductionmentioning
confidence: 99%