In: Aquatic Geochemistry, 2015, vol. 21, no. 2-4, p. 331-342
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In: Analytical and Bioanalytical Chemistry, 2015, vol. 407, no. 14, p. 4035-4044
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In: Analytical and Bioanalytical Chemistry, 2015, vol. 407, no. 20, p. 5977-5986
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In: Inorganic Chemistry, 2009, vol. 48, no. 18, p. 8965-8970
The reduction of (Et(4)N)[Re(III)Br(4)(CO)(2)] (1) by 0.5 equiv of tetrakis- dimethylaminoethylene in acetonitrile yields directly the air-stable, 17-electron Re(II) synthon (Et(4)N)(2)[Re(II)Br(4)(CO)(2)] (2) in nearly quantitative yield. The versatility of 2 as a synthon for Re(II) chemistry was demonstrated by substitution reactions of [Re(II)Br(4)(CO)(2)](2-) with different mono-, bi-,...
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In: RSC Advances, 2021, vol. 11, p. 7511-7520
New synthetic routes to aerobically stable and substitutionally labile α-diimine rhenium(I) dicarbonyl complexes are described. The molecules are prepared in high yield from the cis–cis–trans-[Re(CO)2(tBu2bpy)Br2]− anion (2, where tBu2bpy is 4,4′- di-tert-butyl-2,2′-bipyridine), which can be isolated from the one electron reduction of the corresponding 17-electron complex (1)....
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In: The Journal of Organic Chemistry, 2020, vol. 85, no. 11, p. 7611–7619
Hydrogenolysis of tertiary benzylic alcohols on palladium on carbon (Pd/C) generally proceeds with inversion of configuration. However, little is known about the hydrogenolysis mechanism of primary and secondary benzylic alcohols. Literature precedents suggest that these substrates may interact differently with the catalyst. To study the mechanism, we synthesized a pair of deuterated...
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In: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2020, vol. 237, p. 118416
The paper presents the synthesis and characterization of two 4-substituted phthalimide 2-hydroxy-Schiff bases containing salicylic (4) and 2-hydroxy-1-naphthyl (5) moieties. The structural differences of 2-hydroxyaryl substituents, resulting in different enol/keto tautomeric behaviour, depending on the solvent environment were studied by absorption UV–Vis spectroscopy. Compound 5 is...
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In: Topics in Catalysis, 2014, vol. 57, no. 10-13, p. 843-851
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In: Topics in Catalysis, 2014, vol. 57, no. 14-16, p. 1256-1264
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In: Journal of Nanoparticle Research, 2014, vol. 16, no. 10, p. 1-11
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