Synthesis and Spectroscopic Properties of Novel Fluorescent Compounds Containing Bis-pyrazole Ring

被引：7

作者：

Ren, Tiegang ^{[1
]}

Wang, Jie ^{[1
]}

Li, Guihui ^{[2
]}

Li, Yongzhe ^{[1
]}

机构：

[1] Henan Univ, Coll Chem & Chem Engn, Fine Chem & Engn Res Inst, Kaifeng 475004, Peoples R China

[2] Henan Univ, Key Lab, Minist Educ Special Funct Mat, Kaifeng 475004, Peoples R China

来源：

JOURNAL OF FLUORESCENCE | 2014年 / 24卷 / 04期

关键词：

Pyrazoline derivative; Pyrazole group; Synthesis; Ion recognition; Pectroscopic properties; Co2+;

D O I：

10.1007/s10895-014-1395-y

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

A series of pyrazoline derivatives containing pyrazole group were synthesized and characterized by means of H-1 NMR, FT-IR, MS and elemental analysis, and their UV-vis absorption behavior and fluorescent properties were also measured. Moreover, the influence of metal ions on spectral properties of synthetic products was examined with compound A (5) as an example. It has been found that all synthetic pyrazoline derivatives show two remarkable absorption peaks at about 260 and 360 nm and the maximum emission peak at 445-467 nm. Especially, the joined of Co2+ can quench the fluorescence of compound A (5) obviously.

引用

页码：1149 / 1157

页数：9

共 17 条

[1]

Babu V. Harinadha, 2007, Indian Journal of Pharmaceutical Sciences, V69, P470

[2] Modulated photophysics of 3-pyrazolyl-2-pyrazoline derivative entrapped in micellar assembly [J].

Banerjee, Paltu ;

Pramanik, Smritimoy ;

Sarkar, Arindam ;

Bhattacharya, Subhash Chandra .

JOURNAL OF PHYSICAL CHEMISTRY B, 2008, 112 (24) :7211-7219

[3] Synthesis and in vitro selective anti-Helicobacter pylori activity of pyrazoline derivatives [J].

Chimenti, F ;

Bizzarri, B ;

Manna, F ;

Bolasco, A ;

Secci, D ;

Chimenti, P ;

Granese, A ;

Rivanera, D ;

Lilli, D ;

Scaltrito, MM ;

Brenciaglia, MI .

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (03) :603-607

[4] Synthesis, molecular modeling studies and selective inhibitory activity against MAO of N1-propanoyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives [J].

Chimenti, Franco ;

Fioravanti, Rossella ;

Bolasco, Adriana ;

Manna, Fedele ;

Chimenti, Paola ;

Secci, Daniela ;

Rossi, Francesca ;

Turini, Paola ;

Ortuso, Francesco ;

Alcaro, Stefano ;

Cardia, Maria Cristina .

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2008, 43 (10) :2262-2267

[5] Design, synthesis, and in vitro hMAO-B inhibitory evaluation of some 1-methyl-3,5-diphenyl-4,5-dihydro-1H-pyrazoles [J].

Fioravanti, Rossella ;

Desideri, Nicoletta ;

Biava, Mariangela ;

Monaco, Luca Proietti ;

Grammatica, Laura ;

Yanez, Matilde .

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2013, 23 (18) :5128-5130

[6]

Kumar Suresh, 2009, Recent Pat Antiinfect Drug Discov, V4, P154

[7] Inhibition of amine oxidases activity by 1-acetyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives [J].

Manna, F ;

Chimenti, F ;

Bolasco, A ;

Secci, D ;

Bizzarri, B ;

Befani, O ;

Turini, P ;

Mondovì, B ;

Alcaro, S ;

Tafi, A .

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2002, 12 (24) :3629-3633

[8]

McCann SF, 2001, PEST MANAG SCI, V57, P153, DOI 10.1002/1526-4998(200102)57:2<153::AID-PS288>3.0.CO

[9]

2-O

[10] Synthesis and antimicrobial activity of 1-(4-aryl-2-thiazolyl)-3-(2-thienyl)-5-aryl-2-pyrazoline derivatives [J].

Ozdemir, Ahmet ;

Turan-Zitouni, Gulhan ;

Kaplancikli, Zafer Asim ;

Revial, Gilbert ;

Guven, Kiymet .

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2007, 42 (03) :403-409

← 1 2 →