journal article·2011-09-01

1-Substituted Tetrazole-5-thiol-Capped Noble Metal Nanoparticles

Maria N. Nichick, Sergei V. Voitekhovich, Vladimir Lesnyak, Vitaly E. Matulis, Ryma A. Zheldakova, Anatoly I. Lesnikovich, Oleg A. Ivashkevich

The Journal of Physical Chemistry C· Volume 115· Issue 34
Publisher page

Abstract

Stable and nearly monodispersed silver, palladium, and platinum nanoparticles with an average size of 2–4 nm were synthesized by the reduction of metal precursors (CF 3 COOAg, [NMeAlk 3 ] 2 MCl 4, where M = Pd, Pt) in a biphasic toluene–water system in the presence of easily available 1-R-tetrazole-5-thiols (R = ethyl, tert -butyl, 1-adamantyl, and phenyl) characterized by low carbon content and unique thermal behavior. The obtained noble metal nanoparticles capped with tetrazole-5-thiols were characterized by TEM, TGA, UV–vis, and FTIR spectroscopy. Based on quantum-chemical calculations, preferred coordination mode of the ligands under their binding with surfaces of nanoparticles, namely N(4), S-bridging was proposed. The synthesized silver nanoparticles capped with 1-phenyltetrazole-5-thiol were found to have antifungal and antimicrobial activity against various bacterial strains.
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Research context

OpenAlex topics: Synthesis of Tetrazole Derivatives · Nanoparticles: synthesis and applications · Nanomaterials for catalytic reactions

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Research Institute for Physical Chemical Problems of Belarusian State University, 220030 Minsk, Leningradskaya 14, Belarus

Physical Chemistry, TU Dresden, Bergstrasse 66b, 01062 Dresden, Germany

Microbiology Department, Faculty of Biology, Belarusian State University, 220108 Minsk, Kurchatova 10, Belarus

References (38)

Show source-provided references
1. Talapin D. V. · Chem. Rev. · 2010 · 110 · 38910.1021/cr900137k ↗
2. Gijs M. A. M. · Chem. Rev. · 2010 · 110 · 151810.1021/cr9001929 ↗
3. Goesmann H. · Angew. Chem., Int. Ed. · 2010 · 49 · 136210.1002/anie.200903053 ↗
4. Sperling R. A. · Phil. Trans. Math. Phys. Eng. Sci. · 2010 · 368 · 1333
5. Green M. · J. Mater. Chem. · 2010 · 20 · 579710.1039/c0jm00007h ↗
6. Ostrovskii V. A. · 2008 · 6 · 25710.1016/B978-008044992-0.00517-4 ↗
7. Voitekhovich S. V. · Chem. Mater. · 2008 · 20 · 454510.1021/cm800936c ↗
8. Nichick M. N. · Polyhedron · 2009 · 28 · 313810.1016/j.poly.2009.07.023 ↗
9. Murray, C. B.; Shevchenko, E.; Talapin, D. V.Nanomaterials with Tetrazole-Based Removable Stabilizing Agents. U.S. Patent US 2007/0057255 A1, March 15, 2007.
10. Rogach A. L. · J. Phys. Chem. C · 2007 · 111 · 1462810.1021/jp072463y ↗
11. Gaponik N. · Phys. Chem. Chem. Phys. · 2010 · 12 · 868510.1039/c000916d ↗
12. Lesnyak V. · ACS Nano · 2010 · 4 · 409010.1021/nn100563c ↗
13. 10.1021/ja202068s10.1021/ja202068s ↗
14. Gaponik P. N. · Russ. Chem. Rev. · 2006 · 75 · 50710.1070/RC2006v075n06ABEH003601 ↗
15. Herr R. J. · Bioorg. Med. Chem. · 2002 · 10 · 337910.1016/S0968-0896(02)00239-0 ↗
16. Ziegler C. · Z. Phys. Chem. · 2011 · 225 · 36310.1524/zpch.2011.0049 ↗
17. Kocienski P. J. · Synlett · 2000 · 365
18. Becke A. D. · J. Chem. Phys. · 1993 · 98 · 564810.1063/1.464913 ↗
19. Petersson G. A. · J. Chem. Phys. · 1991 · 94 · 608110.1063/1.460447 ↗
20. Hay P. J. · J. Chem. Phys. · 1985 · 82 · 29910.1063/1.448975 ↗
21. Sandhyarani N. · Chem. Mater. · 2000 · 12 · 10410.1021/cm990429t ↗
22. Cai M. · Appl. Surf. Sci. · 2004 · 226 · 42210.1016/j.apsusc.2003.10.046 ↗
23. Wilcoxon J. · J. Phys. Chem. B · 2009 · 113 · 264710.1021/jp806930t ↗
24. Tatumi R. · Chem. Commun. · 2006 · 334910.1039/B605390B ↗
25. Lin C.-S. · J. Colloid Interface Sci. · 2006 · 229 · 67810.1016/j.jcis.2006.03.003 ↗
26. Gómez-Zavaglia A. · J. Mol. Struct. · 2006 · 786 · 18210.1016/j.molstruc.2005.08.019 ↗
27. Voitekhovich S. V. · Eur. J. Inorg. Chem. · 2010 · 538710.1002/ejic.201000735 ↗
28. Yoon J. · J. Chem. Phys. · 2000 · 112 · 933510.1063/1.481553 ↗
29. Dai D. G. · Chem. Phys. Lett. · 1991 · 184 · 58910.1016/0009-2614(91)80039-Z ↗
30. Whitcomb D. R. · J. Coord. Chem. · 2006 · 59 · 125310.1080/00958970500472937 ↗
31. Ilie A. · Phosphorus, Sulfur, Silicon · 2011 · 186 · 38910.1080/10426507.2010.549020 ↗
32. Wang Y.-L. · Z. Anorg. Allg. Chem. · 2006 · 632 · 16710.1002/zaac.200500342 ↗
33. Tong M. C. · J. Phys. Chem. B · 2006 · 110 · 1923810.1021/jp0631174 ↗
34. Rai M. · Biotechn. Adv. · 2009 · 27 · 7610.1016/j.biotechadv.2008.09.002 ↗
35. Jain J. · Mol. Pharm. · 2009 · 6 · 138810.1021/mp900056g ↗
36. Morones J. R. · Nanotechnology · 2005 · 16 · 234610.1088/0957-4484/16/10/059 ↗
37. Panáček A. · J. Phys. Chem. B · 2006 · 110 · 1624810.1021/jp063826h ↗
38. Pal S. · Appl. Environ. Microbiol. · 2007 · 171210.1128/AEM.02218-06 ↗