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12775-96-1

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12775-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 12775-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,2,7,7 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 12775-96:
(7*1)+(6*2)+(5*7)+(4*7)+(3*5)+(2*9)+(1*6)=121
121 % 10 = 1
So 12775-96-1 is a valid CAS Registry Number.

12775-96-1Relevant articles and documents

E-ALD of Cu nanofilms on Ru/Ta wafers using surface limited redox replacement

Thambidurai, Chandru,Gebregziabiher, Daniel K.,Liang, Xuehai,Zhang, Qinghui,Ivanova, Valentina,Haumesser, Paul-Henri,Stickney, John L.

, p. D466-D471 (2010)

This paper describes the formation of Cu nanofilms on a Ru/Ta-coated wafer using electrochemical atomic layer deposition (E-ALD). The initial steps involved cleaning and oxide removal from the Ru/Ta substrate using ultrahigh vacuum electrochemical system. Auger spectroscopy was used to follow the relative amounts of oxygen, Ru, and Cu on the wafer: as-received, after electrochemical treatment, after ion bombardment, and after Cu deposition. An automated flow cell electrodeposition system was employed to grow Cu nanofilms with up to 200 cycles using surface limited redox replacement (SLRR) reaction. The open-circuit potential was used to follow the exchange of Pb for Cu in the SLRR reaction. Electron probe microanalysis was used to determine the homogeneity of the Cu films. The use of a complexing agent (citrate) greatly improved the homogeneity. Different concentrations of citrate were investigated, containing 2 or 4 mM citrate. Atomic force microscopy images of the Cu films showed the ingress morphology to be the same as the egress when 4 mM citrate was used. A prominent Cu(111) peak was displayed in the X-ray diffraction pattern for 200 cycles of Cu grown on the Ru/Ta-coated wafer.

Synthesis of an Ag@AgCl catalyst with amorphous copper as the support and its catalytic performance in the reduction of 4-nitrophenol

Bao, Lei,Dong, Hanfeng,Fu, Xucheng,Gan, Wei,Hao, Hequn,Liu, Luying,Qin, Chenchen,Wang, Yujuan,Zhang, Jian

, p. 551 - 557 (2020/07/24)

The support used in a composite catalyst has an important influence on the catalytic performance of the catalyst. Amorphous metals have good electron-transfer properties and the presence of defect structures on the surface will introduce additional active sites and should be excellent catalyst supports. In this study, an Ag@AgCl composite catalyst with amorphous Cu (a-Cu) as the support is prepared by a two-step precipitation method at room temperature and a light irradiation reduction method. Compared to the Ag@AgCl and a-Cu, the catalytic rate of the Ag@AgCl/a-Cu composite catalytic rate was 2.04 times and 6.69 times faster during the reduction of 4-NP in NaBH4 aqueous solution. The high-performance catalytic efficiency and reusability of Ag@AgCl/a-Cu may be attributed to the synergistic effect between Ag@AgC and amorphous metal elements. This work may provide an effective reference for the synthesis of high activity catalysts using amorphous metals as supports.

Synthesis, Structure, DFT, and Biological Activity of Metal Complexes of Norfloxacin and Metformin Mixed Ligand

Abbass, L. M.,El-Shwiniy, W. H.,El-Telbany, M.,Sadeek, S. A.,Zordok, W. A.

, p. 1774 - 1782 (2021/11/01)

Abstract: A new series of mixed ligand metal complexes has been synthesized by the reaction of Co(II), Ni(II), Cu(II), Zr(IV), Pd(II), and Cd(II) with norfloxacin (NOR) and metformin hydrochloride (MF) in 1 : 1 : 1 molar ratio. The complexes have been characterized by FT-IR, UV-Vis, and 1H NMR spectra, TG/DTG and elemental analysis, molar conductance, and magnetic susceptibility data. According to FT-IR, NOR chelates with metal ions as a bidentate ligand via one oxygen of the carboxylate group and pyridone oxygen, and MF chelates with metal ions via two imine groups. Complexes have been identified as electrolytes. Electronic and magnetic data have indicated the octahedral structure for all complexes except square planar Pd(II) complex. Antibacterial and antifungal activities of the compounds have been tested against several species, and have indicated higher inhibition against micro-organisms for the metal complexes than the mixed ligands.

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