2018
DOI: 10.1016/j.molstruc.2018.03.008
|View full text |Cite
|
Sign up to set email alerts
|

New copper complexes with bipyrazolic ligands: Synthesis, characterization and evaluation of the antibacterial and catalytic properties

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
9
0

Year Published

2019
2019
2023
2023

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 15 publications
(10 citation statements)
references
References 30 publications
1
9
0
Order By: Relevance
“…Negative shifts of peaks corresponding to carboxyl groups from 1690 cm À1 to 1650 cm À1 were observedi nt he FTIR spectra of CNNS-BTEC-Cu-1, CNNS-BTEC-Cu-3, and CNNS-BTEC-Cu-5, whichr esulted from the coordination interaction betweenc opper(II) and carboxyl groups. [17] Similarr esults were also obtained by conducting XRD measurements (see the Supporting Information, Figure S1). With the increasing ratio of added BTEC, weak peaks ranging from 12.08 to 33.08 emerged in the XRD patterns of CNNS-BTEC-Cu-3 and CNNS-BTEC-Cu-5, which corresponded to the typical XRD pattern of BTEC ( Figure S2).…”
Section: Resultssupporting
confidence: 76%
See 1 more Smart Citation
“…Negative shifts of peaks corresponding to carboxyl groups from 1690 cm À1 to 1650 cm À1 were observedi nt he FTIR spectra of CNNS-BTEC-Cu-1, CNNS-BTEC-Cu-3, and CNNS-BTEC-Cu-5, whichr esulted from the coordination interaction betweenc opper(II) and carboxyl groups. [17] Similarr esults were also obtained by conducting XRD measurements (see the Supporting Information, Figure S1). With the increasing ratio of added BTEC, weak peaks ranging from 12.08 to 33.08 emerged in the XRD patterns of CNNS-BTEC-Cu-3 and CNNS-BTEC-Cu-5, which corresponded to the typical XRD pattern of BTEC ( Figure S2).…”
Section: Resultssupporting
confidence: 76%
“…The intensity of peaks corresponding to carboxyl groups in CNNS‐BTEC‐Cu‐1, CNNS‐BETC‐Cu‐3, and CNNS‐BTEC‐Cu‐5 increased with the increasing ratio of BTEC in these samples. Negative shifts of peaks corresponding to carboxyl groups from 1690 cm −1 to 1650 cm −1 were observed in the FTIR spectra of CNNS‐BTEC‐Cu‐1, CNNS‐BTEC‐Cu‐3, and CNNS‐BTEC‐Cu‐5, which resulted from the coordination interaction between copper(II) and carboxyl groups . Similar results were also obtained by conducting XRD measurements (see the Supporting Information, Figure S1).…”
Section: Resultsmentioning
confidence: 99%
“…The first step was similar to the previous one, 1,3-DCH reacted with two molecules of the corresponding pyrazole derivative. The final Cu(II) complex showed good catalytic properties in the oxidation of catechol [126]. Cooper (II) complexes were also obtained via the synthesis of a bipyrazolic ligand, bearing two carboxyl groups ( Figure 12).…”
Section: Synthesis Of Polynuclear Metalsmentioning
confidence: 99%
“…The first step was similar to the previous one, 1,3-DCH reacted with two molecules of the corresponding pyrazole derivative. The final Cu(II) complex showed good catalytic properties in the oxidation of catechol [126]. Polynuclear metals have many potential applications, e.g., therapeutic agents (e.g., photocleavage of DNA), photovoltaic components, photocatalysts, magnetic materials and tuneable chemical sensors [127][128][129][130].…”
Section: Synthesis Of Polynuclear Metalsmentioning
confidence: 99%
“…Chlorantraniliprole, an insecticide developed by DuPont company, contains a pyrazole ring. Pyrazole derivatives possess diverse biological activities, such as antibacterial , G protein‐coupled receptor 52 (GPR52) agonists , nematocidal , antimitotic , antidiabetic , antifungal , and others.…”
Section: Introductionmentioning
confidence: 99%