2011
DOI: 10.1016/j.arabjc.2010.06.012
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis of some novel heterocyclic dyes derived from pyrazole derivatives

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
11
0

Year Published

2016
2016
2024
2024

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 38 publications
(11 citation statements)
references
References 19 publications
0
11
0
Order By: Relevance
“…Total dyeing time was 90 min. It was then cooled to 60 °C and then after washing, dyed samples were rinsed and dried …”
Section: Methodsmentioning
confidence: 99%
“…Total dyeing time was 90 min. It was then cooled to 60 °C and then after washing, dyed samples were rinsed and dried …”
Section: Methodsmentioning
confidence: 99%
“…The infrared spectra were recorded on Perkin-Elmer FTIR 1430 spectrophotometer using the KBr disk technique. The 1 H NMR and 13 C NMR spectra were recorded on a Bruker AC spectrometer (300 MHz) at 25˚C in DMSO-d 6 with TMS as internal standard and chemical shifts are reported in ppm as δ values. Reactions were conducted under microwave irradiation in closed vessels under magnetic stirring in a Synthos 3000 (Anton Paar) microwave with dual magnetrons system and with maximum power of 1000 W. Mass spectra were measured on a Finnigan MAT 8222 EX mass spectrometer at 70 eV.…”
Section: Chemistrymentioning
confidence: 99%
“…2) Method B: To a solution of 1-phenyl-3-pyridyl-5-pyrazolone 1 (4.74 g, 20 mmole) and acetonitrile (20 ml) add a solution of NBSc (N-bromo sacharrine) (5.2 g, 20 mmole) in acetonitrile (10 ml) dropwise at room temperature with stirring for 4 h. The formed precipitate was filtrated; washed with chloroform, dried and crystallized from ethanol to give compound 2, (87% yield) with same melting and mixed m.p. IR (KBr) υ/cm −1 = 2980 (CH aliph ), 1658 (C=O), 1558 (C=N), 748 (C-Br); 1 H NMR (DMSO): δ ppm = 7 -7.64 (m, 5H, ph-H), 7.66 -8.83 (m, 4H, H-pyridine); 13 C NMR (DMSO): δ ppm = 49 (C 4 pyridine), 120 -132 (Ar-C), 124 -152 (py-C), 155 (C 4 pyridine), 160 (C=O); Anal. Cald.…”
Section: Preparation Of 4-bromo-1-phenyl-3-(pyridin-3-yl)-1h-pyrazol-mentioning
confidence: 99%
See 1 more Smart Citation
“…Several attempts for creating suitable functional groups in PET substrates were made in the past [23,24]. Most recently, novel pyrazolotriazine and pyrazolylpyrazoloneazo dyes have been synthesized and were applied to polyester by using a disperse dyeing technique, which is commonly used for dyeing polyester, to study the antibacterial activity of the above azo dyes [25]. Subsequently, different approaches have been used by researchers to impart antimicrobial activity to the polyester based textile materials [26][27][28][29][30].…”
Section: Introductionmentioning
confidence: 99%