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EN
A novel two-di men sional cop per com plex con nected by dual EO- and sin gle EE-azide bridges, [Cu(AMP)(mi1,1-N3)(mi1,3-N3)]n (1) (AMP = 2-(aminomethyl)pyridine), has been syn the sized and characterized by IR spectrum, elemental analysis, and single crystal X-ray determination. Each Cu atom is six-coordinate in an octahedral configuration in - volving two N atoms of AMP ligand and four N atoms from four azide bridges. The N atom in EO-azide bridge occupies equatorial plane in one Cu(II) center and axial position in the other Cu(II) center. The Jahn-Teller effect on the octahedral geometry of Cu(II) plays a prominent role in length en ing the Cu-N distances in axial position. Magnetic susceptibility has been investigated and reveals that azides mediate antiferromagnetic interactions with J = –16.9 cm–1 and J'= –0.83 cm–1, respectively for EO and EE bridges.
EN
Two new compounds, Co(bpm)2(N3)2 (1) and {[Ni(bpm)2(H2O)2][Ni(bpm)2(N3)2]}(ClO4)2 (2), where bpm refers to bis(pyrazol-1-yl)methane, have been prepared and characterized by elemental analyses, IR, UV-Vis spectra and X-ray diffraction. Crystal data for 1: monoclinic, space group P21/n with a = 10.394(4), b =14.410(5), c = 12.591(4) Alfa,Beta = 91.194(7)°, V =1885.6(11) Alfa3 and Z= 4. Crystal data for 2: triclinic, space group P1with a = 8.7673(6), b = 8.9618(6), c = 13.5653(9) Alfa, alfa = 84.6040(10) , beta= 84.4230(10) , _ = 79.6040(10), V = 1040.19(12) Alfa3 and Z = 1. Complex 1 is a neutral monomer molecule, in which CoII ion is coordinated by four nitrogen atoms from two chelating bpm and two terminal azide ligands to form a cis-octahedral configuration. However, compound 2 is composed of a neutral [Ni(bpm)2(N3)2] entity, one [Ni(bpm)2(H2O)2]2+ cation and perchlorate anions, in which the neutral Ni(bpm)2(N3)2 entity is in a trans-six-coordinated configuration. The uncoordinated terminal nitrogen atom of azide forms O-H.....N hydrogen bonds with the coordinated H2O molecule to afford a one-dimensional chain structure.
EN
The influence of microwave energy on the rate of cleavage of-C-S- and -S-S- bonds by azide ions was investigated. It was found that microwaves do not accelerate the split of -C-S- bond, whereas the cleavage of-S-S- bond takes place faster but the reproducibility of this reaction is very poor and microwave technique is not recommended for quantitative determination.
PL
Badano wpływ energii mikrofalowej na szybkość rozszczepienia wiązania -C-S-i -S-S- przez jony azydkowe. Stwierdzono, że mikrofale nie przyspieszają zerwania wiązania -C-S-, natomiast rozszczepienie wiązania -S-S- zachodzi szybciej, jednak niepowtarzalność procesu wyklucza możliwość stosowania tej techniki w analizie ilościowej.
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