Reaction of metals with benzenediazonium tetrafluoroborate in aprotic solvents

被引:2
|
作者
Koval'chuk, Eugen P. [1 ]
Reshetnyak, Oleksandr V. [1 ]
Pereviznyk, Orest B. [1 ]
Marchuk, Iryna E. [1 ]
Smetanets'kyj, Vasyl Ya. [1 ]
Blazejowski, Jerzy [2 ]
机构
[1] Ivan Franko Natl Univ Lviv, Fac Chem, Dept Phys & Colloid Chem, UA-79005 Lvov, Ukraine
[2] Univ Gdansk, Fac Chem, Dept Phys Chem, PL-80952 Gdansk, Poland
来源
关键词
Benzenediazonium tetrafluoroborate; Electrochemical reduction; Copper; Ionization-dissolution; Complexing; AROMATIC DIAZONIUM SALTS; WALLED CARBON NANOTUBES; ELECTROCHEMICAL REDUCTION; ORGANIC LAYERS; ARYLDIAZONIUM SALTS; BETA-CYCLODEXTRIN; SURFACES; ELECTRODES; ION; COMPLEXES;
D O I
10.2478/s11532-010-0026-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reaction of metals and glassy carbon with benzenediazonium tetrafluoroborate (BDFB) in aprotic solvents has been studied. During contact of Pt, Au, Ag, Pd, or V with glassy carbon in concentrated diazonium salt solution no change of color was observed. For Al, Ca, Cr, Cu, Fe, Ga, In, Mg, Li, Na, or Zn the process was accompanied by a rapid solution color change, rapid N-2 release and the loss of metal sample mass. The copper metal ionization-dissolution was studied by ultraviolet and visible absorption spectroscopy, along with gravimetric and volumetric measurements. A dissolution mechanism was proposed based on kinetic, infrared, and X-ray diffraction data. The 432 nm absorption band appearing after Cu-BDFB reaction indicates formation of the mixed complex [Cu(N2C6H5 center dot(N C-CH3)(3)](+) where the copper atom is covalently bonded to the azophenyl radical and coordinated to acetonitrile (ACN). This complex is thermodynamically unstable and decomposes slowly to a colorless crystalline and a black amorphous phase. The crystalline phase was identified as [Cu(NC-CH3)(4)]BF4. The amorphous phase is a mixture of products formed by azophenyl and phenyl radical condensation.
引用
收藏
页码:652 / 661
页数:10
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