Correlation between catalytic activity and surface ligands of monolayer protected gold nanoparticles

Journal of Colloid and Interface Science

Volumn 368, Issue 1, 2012, Pages 77-85

  Biswas, Mrinmoy ^a   Dinda, Enakshi ^a   Rashid, Md Harunar ^a   Mandal, Tarun K ^a  

^a DEPARTMENT OF MATERIALS SCIENCE   (India)

Author keywords

4 Nitrophenol; Catalysts; Gold nanoparticles; Ligand capped; Thin film

Indexed keywords

11-MERCAPTOUNDECANOIC ACID; 4-NITROPHENOL; ALKANETHIOLS; ALKYL AMINES; ALKYL CHAIN LENGTHS; ANCHORING GROUPS; BOROHYDRIDE REDUCTIONS; CATALYTIC PROPERTIES; FUNCTIONALIZATIONS; FUNCTIONALIZED; GLASS SUBSTRATES; GOLD NANOPARTICLES; GRAFT DENSITY; IN-DEPTH STUDY; LIGAND MOLECULES; LIGAND-CAPPED; MODEL REACTIONS; MONOLAYER-PROTECTED GOLD NANOPARTICLES; POTASSIUM FERRICYANIDE; SIZE AND SHAPE; SODIUM THIOSULFATE; STABILIZING LIGANDS; SURFACE LIGANDS;

AGGLOMERATION; CATALYSTS; GOLD; LIGANDS; MONOLAYERS; NANOPARTICLES; POTASSIUM; REDOX REACTIONS; SODIUM; SUBSTRATES; THIN FILMS;

CATALYST ACTIVITY;

11 MERCAPTOUNDECANOL; 4 NITROPHENOL; ALIPHATIC AMINE; ALKANE; ALKANETHIOL; ALKANOL; BORANE DERIVATIVE; GOLD NANOPARTICLE; MERCAPTOPURINE; MERCAPTOUNDECANOIC ACID; POTASSIUM FERRICYANIDE; SODIUM THIOSULFATE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; FILM; NANOCATALYST; OXIDATION REDUCTION REACTION; PRIORITY JOURNAL; SURFACE PROPERTY; SUSPENSION; SYNTHESIS;

EID: 84855831653     PISSN: 00219797     EISSN: 10957103     Source Type: Journal    
DOI: 10.1016/j.jcis.2011.10.078     Document Type: Article

References (44)

1. Corti C.W., Holliday R.J., Thompson D.T. Top. Catal. 2007, 44:331.
2. Comotti M., Della Pina C., Matarrese R., Rossi M. Angew. Chem. Int. Ed. 2004, 43:5812.
3. Dinda E., Rashid M.H., Biswas M., Mandal T.K. Langmuir 2010, 26:17568.
4. Li M., Hu L., Cao X.Q., Hong H.Y., Lu J.M., Gu H.W. Chem.-Eur. J. 2011, 17:2763.
5. Lv W.P., Wang Y., Feng W.Q., Qi J.J., Zhang G.L., Zhang F.B., Fan X.B. J. Mater. Chem. 2011, 21:6173.
6. Mitsudome T., Arita S., Mori H., Mizugaki T., Jitsukawa K., Kaneda K. Angew. Chem.-Int. Ed. 2008, 47:7938.
7. Murugadoss A., Chattopadhyay A. Nanotechnology 2008, 19:015603.
8. Narayanan R., El-Sayed M.A. J. Am. Chem. Soc. 2004, 126:7194.
9. Polshettiwar V., Varma R.S. Green Chem. 2010, 12:743.
10. Rashid H., Mandal T.K. J. Phys. Chem. C 2007, 111:16750.
11. Rashid M.H., Mandal T.K. Adv. Funct. Mater. 2008, 18:2261.
12. Wang L., Yamauchi Y. Chem. Mater. 2011, 23:2457.
13. Pradhan N., Pal A., Pal T. Langmuir 2001, 17:1800.
14. Rashid M.H., Bhattacharjee R.R., Kotal A., Mandal T.K. Langmuir 2006, 22:7141.
15. Selvaraju T., Das J., Han S.W., Yang H. Biosens. Bioelectron. 2008, 23:932.
16. Haruta M. Catal. Today 1997, 36:153.
17. De Rogatis L., Cargnello M., Gombac V., Lorenzut B., Montini T., Fornasiero P. ChemSusChem 2010, 3:24.
18. Fang W.H., Chen J.S., Zhang Q.H., Deng W.P., Wang Y. Chem. Eur. J. 2011, 17:1247.
19. Chang Y.C., Chen D.H. J. Hazard. Mater. 2009, 165:664.
20. Chen X., Zhao D.Y., An Y.L., Zhang Y., Cheng J., Wang B.L., Shi L.Q. J. Colloid Interface Sci. 2008, 322:414.
21. He H.K., Gao C. Sci. China-Chem. 2011, 54:397.
22. Lee J., Park J.C., Song H. Adv. Mater. 2008, 20:1523.
23. Mori K., Kumami A., Tomonari M., Yamashita H. J. Phys. Chem. C 2009, 113:16850.
24. Saha S., Pal A., Kundu S., Basu S., Pal T. Langmuir 2009, 26:2885.
25. Shin K.S., Choi J.Y., Park C.S., Jang H.J., Kim K. Catal. Lett. 2009, 133:1.
26. Tang J.A., Tang D.P., Su B.L., Huang J.X., Qiu B., Chen G.N. Biosens. Bioelectron. 2011, 26:3219.
27. Wei D.W., Ye Y.Z., Jia X.P., Yuan C., Qian W.P. Carbohyd. Res. 2010, 345:74.
28. Koga H., Kitaoka T. Chem. Eng. J. 2011, 168:420.
29. Hariprasad E., Radhakrishnan T.P. Chem. Eur. J. 2010, 16:14378.
30. Cortial G., Siutkowski M., Goettmann F., Moores A., Boissiere C., Grosso D., Le Floch P., Sanchez C. Small 2006, 2:1042.
31. Jana D., Dandapat A., De G. Langmuir 2010, 26:12177.
32. Liu J.C., Qin G.W., Raveendran P., Kushima Y. Chem. Eur. J. 2006, 12:2132.
33. Yin H.M., Zhou C.Q., Xu C.X., Liu P.P., Xu X.H., Ding Y. J. Phys. Chem. C 2008, 112:9673.
34. Daniel M.C., Astruc D. Chem. Rev. 2004, 104:293.
35. Zaupa G., Mora C., Bonomi R., Prins L.J., Scrimin P. Chem. Eur. J. 2011, 17:4879.
36. Cruickshank A.C., Downard A.J. Electrochim. Acta 2009, 54:5566.
37. Love J.C., Estroff L.A., Kriebel J.K., Nuzzo R.G., Whitesides G.M. Chem. Rev. 2005, 105:1103.
38. Vericat C., Vela M.E., Benitez G., Carro P., Salvarezza R.C. Chem. Soc. Rev. 2010, 39:1805.
39. Li D., Sun C.Y., Huang Y.J., Li J.H., Chen S.W. Sci. China Ser. B 2005, 48:424.
40. Bhattacharjee R.R., Mandal T.K. J. Colloid Interface Sci. 2007, 307:288.
41. Laaksonen T., Ahonen P., Johans C., Kontturi K. ChemPhysChem 2006, 7:2143.
42. Mandal T.K., Fleming M.S., Walt D.R. Nano Lett. 2002, 2:3.
43. Lopez-Sanchez J.A., Dimitratos N., Hammond C., Brett G.L., Kesavan L., White S., Miedziak P., Tiruvalam R., Jenkins R.L., Carley A.F., Knight D., Kiely C.J., Hutchings G.J. Nat. Chem. 2011, 3:551.
44. Veres M., Perevedentseva E., Karmenyan A.V., Tóth S., Koós M. Phys. Status Solidi C 2010, 7:1211.