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Volumn 3, Issue 1, 2013, Pages 55-69

Glycerol: A promising green solvent and reducing agent for metal-catalyzed transfer hydrogenation reactions and nanoparticles formation

Author keywords

Glycerol; Green solvent; Hydrogen donor; Metal catalysis; Metal nanoparticles; Reduction reactions; Transfer hydrogenation

Indexed keywords


EID: 84885880358     PISSN: None     EISSN: 20763417     Source Type: Journal    
DOI: 10.3390/app3010055     Document Type: Review
Times cited : (113)

References (82)
  • 1
    • 38549149213 scopus 로고    scopus 로고
    • Chemoselective catalytic conversion of glycerol as a biorenewable source to valuable commodity chemicals
    • Zhou, C.-H.; Beltramini, J.N.; Fan, Y.-X.; Lu, G.Q. Chemoselective catalytic conversion of glycerol as a biorenewable source to valuable commodity chemicals. Chem. Soc. Rev. 2008, 37, 527-549
    • (2008) Chem. Soc. Rev , vol.37 , pp. 527-549
    • Zhou, C.-H.1    Beltramini, J.N.2    Fan, Y.-X.3    Lu, G.Q.4
  • 4
    • 34447129755 scopus 로고    scopus 로고
    • Chemical routes for the transformation of biomass into chemicals
    • Corma, A.; Iborra, S.; Velty, A. Chemical routes for the transformation of biomass into chemicals. Chem. Rev. 2007, 107, 2411-2502
    • (2007) Chem. Rev , vol.107 , pp. 2411-2502
    • Corma, A.1    Iborra, S.2    Velty, A.3
  • 5
    • 37549070353 scopus 로고    scopus 로고
    • The glycerin glut: Options for the value-added conversion of crude glycerol resulting from biodiesel production
    • Johnson, D.T.; Taconi, K.A. The glycerin glut: Options for the value-added conversion of crude glycerol resulting from biodiesel production. Environ. Prog. 2007, 26, 338-348
    • (2007) Environ. Prog , vol.26 , pp. 338-348
    • Johnson, D.T.1    Taconi, K.A.2
  • 6
    • 53749088913 scopus 로고    scopus 로고
    • Rational design of solid catalysts for the selective use of glycerol as a natural organic building block
    • Jérôme, F.; Pouilloux, Y.; Barrault, J. Rational design of solid catalysts for the selective use of glycerol as a natural organic building block. ChemSusChem 2008, 1, 586-613
    • (2008) ChemSusChem , vol.1 , pp. 586-613
    • Jérôme, F.1    Pouilloux, Y.2    Barrault, J.3
  • 7
    • 37849012760 scopus 로고    scopus 로고
    • Improved utilisation of renewable resources: New important derivatives of glycerol
    • Behr, A.; Eilting, J.; Irawadi, K.; Leschinski, J.; Lindner, F. Improved utilisation of renewable resources: New important derivatives of glycerol. Green Chem. 2008, 10, 13-30
    • (2008) Green Chem , vol.10 , pp. 13-30
    • Behr, A.1    Eilting, J.2    Irawadi, K.3    Leschinski, J.4    Lindner, F.5
  • 9
    • 57349088282 scopus 로고    scopus 로고
    • Glycerol: A promising and abundant carbon source for industrial microbiology
    • Da Silva, G.P.; Mack, M.; Conteiro, J. Glycerol: A promising and abundant carbon source for industrial microbiology. Biotechnol. Adv. 2009, 27, 30-39
    • (2009) Biotechnol. Adv , vol.27 , pp. 30-39
    • Da Silva, G.P.1    Mack, M.2    Conteiro, J.3
  • 10
    • 68149152164 scopus 로고    scopus 로고
    • Glycerochemistry: New products and processes from glycerin of biodiesel production
    • Mota, C.J.A.; da Silva, C.X.A.; Gonçalves, V.L.C. Glycerochemistry: New products and processes from glycerin of biodiesel production. Quim. Nova 2009, 32, 639-648
    • (2009) Quim. Nova , vol.32 , pp. 639-648
    • Mota, C.J.A.1    da Silva, C.X.A.2    Gonçalves, V.L.C.3
  • 11
    • 78651426175 scopus 로고    scopus 로고
    • Use of hybrid organic-siliceous materials for the selective conversion of glycerol
    • Jérôme, F.; Barrault, J. Use of hybrid organic-siliceous materials for the selective conversion of glycerol. Eur. J. Lipid Sci. Technol. 2011, 113, 118-134
    • (2011) Eur. J. Lipid Sci. Technol , vol.113 , pp. 118-134
    • Jérôme, F.1    Barrault, J.2
  • 12
    • 84655163350 scopus 로고    scopus 로고
    • Novel strategy for the bisbutenolide synthesis via ring-closing metathesis
    • Billamboz, M.; Lageay, J.C.; Hapiot, F.; Monflier, E.; Len, C. Novel strategy for the bisbutenolide synthesis via ring-closing metathesis. Synthesis 2012, 14, 137-143
    • (2012) Synthesis , vol.14 , pp. 137-143
    • Billamboz, M.1    Lageay, J.C.2    Hapiot, F.3    Monflier, E.4    Len, C.5
  • 13
    • 70350005405 scopus 로고    scopus 로고
    • Glycerol reforming for hydrogen production: A review
    • Vaidya, P.D.; Rodrigues, A.E. Glycerol reforming for hydrogen production: A review. Chem. Eng. Technol. 2009, 32, 1463-1469
    • (2009) Chem. Eng. Technol , vol.32 , pp. 1463-1469
    • Vaidya, P.D.1    Rodrigues, A.E.2
  • 15
    • 84857585600 scopus 로고    scopus 로고
    • Hydrogen via stream reforming of liquid biofeedstock
    • Nahar, G.; Dupont, V. Hydrogen via stream reforming of liquid biofeedstock. Biofuels 2012, 3, 167-191
    • (2012) Biofuels , vol.3 , pp. 167-191
    • Nahar, G.1    Dupont, V.2
  • 16
    • 74449084766 scopus 로고    scopus 로고
    • Recent progress on innovative and potential technologies for glycerol transformation into fuel additives: A critical review
    • Rahmat, N.; Abdullah, A.Z.; Mohamed, A.R. Recent progress on innovative and potential technologies for glycerol transformation into fuel additives: A critical review. Renew. Sustain. Energy Rev. 2010, 14, 987-1000
    • (2010) Renew. Sustain. Energy Rev , vol.14 , pp. 987-1000
    • Rahmat, N.1    Abdullah, A.Z.2    Mohamed, A.R.3
  • 20
    • 33847616559 scopus 로고    scopus 로고
    • Alternatives solvents: Shades of green
    • Clark, J.H.; Taverner, S.J. Alternatives solvents: Shades of green. Org. Process Res. Dev. 2007, 11, 149-155
    • (2007) Org. Process Res. Dev , vol.11 , pp. 149-155
    • Clark, J.H.1    Taverner, S.J.2
  • 22
    • 79958847881 scopus 로고    scopus 로고
    • Searching for green solvents
    • Jessop, P.G. Searching for green solvents. Green Chem. 2011, 13, 1391-1398
    • (2011) Green Chem , vol.13 , pp. 1391-1398
    • Jessop, P.G.1
  • 24
    • 33645383062 scopus 로고    scopus 로고
    • Organic chemistry in water
    • Li, C.-J.; Chen, L. Organic chemistry in water. Chem. Soc. Rev. 2006, 35, 68-82
    • (2006) Chem. Soc. Rev , vol.35 , pp. 68-82
    • Li, C.-J.1    Chen, L.2
  • 25
    • 77951227179 scopus 로고    scopus 로고
    • The development of catalytic nucleophilic additions of terminal alkynes in water
    • Li, C.-J. The development of catalytic nucleophilic additions of terminal alkynes in water. Acc. Chem. Res. 2010, 43, 581-590
    • (2010) Acc. Chem. Res , vol.43 , pp. 581-590
    • Li, C.-J.1
  • 26
    • 82355172743 scopus 로고    scopus 로고
    • An efficient and expeditious Fmoc protection of amines and amino acids in aqueous media
    • Gawande, M.B.; Branco, P.S. An efficient and expeditious Fmoc protection of amines and amino acids in aqueous media. Green Chem. 2011, 13, 3355-3359
    • (2011) Green Chem , vol.13 , pp. 3355-3359
    • Gawande, M.B.1    Branco, P.S.2
  • 27
    • 84871794514 scopus 로고    scopus 로고
    • Metal-catalyzed amide bond forming reactions in an environmentally friendly aqueous medium: Nitrile hydrations and beyond
    • García-álvarez, R.; Crochet, P.; Cadierno, V. Metal-catalyzed amide bond forming reactions in an environmentally friendly aqueous medium: Nitrile hydrations and beyond. Green Chem. 2013, 15, 46-66
    • (2013) Green Chem , vol.15 , pp. 46-66
    • García-álvarez, R.1    Crochet, P.2    Cadierno, V.3
  • 28
    • 34547119921 scopus 로고    scopus 로고
    • Glycerol as a green solvent for high product yields and selectivities
    • Wolfson, A.; Dlugy, C.; Shotland, Y. Glycerol as a green solvent for high product yields and selectivities. Environ. Chem. Lett. 2007, 5, 67-71
    • (2007) Environ. Chem. Lett , vol.5 , pp. 67-71
    • Wolfson, A.1    Dlugy, C.2    Shotland, Y.3
  • 29
    • 77954592787 scopus 로고    scopus 로고
    • Glycerol as a sustainable solvent for green chemistry
    • Gu, Y.; Jérôme, F. Glycerol as a sustainable solvent for green chemistry. Green Chem. 2010, 12, 1127-1138
    • (2010) Green Chem , vol.12 , pp. 1127-1138
    • Gu, Y.1    Jérôme, F.2
  • 31
    • 84887931515 scopus 로고    scopus 로고
    • Glycerol-based solvents in organic synthesis
    • Wolfson, A.; Dlugy, C.; Tavor, D. Glycerol-based solvents in organic synthesis. Trends Org. Chem. 2011, 15, 41-50
    • (2011) Trends Org. Chem , vol.15 , pp. 41-50
    • Wolfson, A.1    Dlugy, C.2    Tavor, D.3
  • 32
    • 84903176468 scopus 로고    scopus 로고
    • Glycerol as an Alternative Solvent for Organic Reactions
    • Ali Mohammad, Inamuddin, Eds.; Springer Science & Business Media: Dordrecht, The Netherlands
    • Calvino-Casilda, V. Glycerol as an Alternative Solvent for Organic Reactions. In Green Solvents I: Properties and Applications in Chemistry; Ali Mohammad, Inamuddin, Eds.; Springer Science & Business Media: Dordrecht, The Netherlands, 2012; pp. 187-207
    • (2012) Green Solvents I: Properties and Applications in Chemistry , pp. 187-207
    • Calvino-Casilda, V.1
  • 34
    • 84864182633 scopus 로고    scopus 로고
    • Glycerol as a biodegradable and reusable promoting medium for the catalyst-free one-pot three component synthesis of 4H-pyrans
    • Safaei, H.R.; Shekouhy, M.; Rahmanpur, S.; Shirinfeshan, A. Glycerol as a biodegradable and reusable promoting medium for the catalyst-free one-pot three component synthesis of 4H-pyrans. Green Chem. 2012, 14, 1696-1704
    • (2012) Green Chem , vol.14 , pp. 1696-1704
    • Safaei, H.R.1    Shekouhy, M.2    Rahmanpur, S.3    Shirinfeshan, A.4
  • 35
    • 53849103632 scopus 로고    scopus 로고
    • Glycerol as an efficient promoting medium for organic reactions
    • Gu, Y.; Barrault, J.; Jérôme, F. Glycerol as an efficient promoting medium for organic reactions. Adv. Synth. Catal. 2008, 350, 2007-2012
    • (2008) Adv. Synth. Catal , vol.350 , pp. 2007-2012
    • Gu, Y.1    Barrault, J.2    Jérôme, F.3
  • 37
    • 77956364235 scopus 로고    scopus 로고
    • Palladium-catalyzed cycloisomerization of (Z)-enynols into furans using green solvents: Glycerol vs. water
    • Francos, J.; Cadierno, V. Palladium-catalyzed cycloisomerization of (Z)-enynols into furans using green solvents: Glycerol vs. water. Green Chem. 2010, 12, 1552-1555
    • (2010) Green Chem , vol.12 , pp. 1552-1555
    • Francos, J.1    Cadierno, V.2
  • 38
    • 4243378570 scopus 로고
    • Asymmetric hydrogen transfer reactions promoted by homogeneous transition metal catalysts
    • Zassinovich, G.; Mestroni, G.; Gladiali, S. Asymmetric hydrogen transfer reactions promoted by homogeneous transition metal catalysts. Chem. Rev. 1992, 92, 1051-1069
    • (1992) Chem. Rev , vol.92 , pp. 1051-1069
    • Zassinovich, G.1    Mestroni, G.2    Gladiali, S.3
  • 39
    • 33644661038 scopus 로고    scopus 로고
    • Asymmetric transfer hydrogenation: Chiral ligands and applications
    • Gladiali, S.; Alberico, E. Asymmetric transfer hydrogenation: Chiral ligands and applications. Chem. Soc. Rev. 2006, 35, 226-236
    • (2006) Chem. Soc. Rev , vol.35 , pp. 226-236
    • Gladiali, S.1    Alberico, E.2
  • 40
    • 33644660116 scopus 로고    scopus 로고
    • Mechanistic aspects of transition metal-catalyzed hydrogen transfer reactions
    • Samec, J.S.M.; Bäckvall, J.-E.; Andersson, P.G.; Brandt, P. Mechanistic aspects of transition metal-catalyzed hydrogen transfer reactions. Chem. Soc. Rev. 2006, 35, 237-248
    • (2006) Chem. Soc. Rev , vol.35 , pp. 237-248
    • Samec, J.S.M.1    Bäckvall, J.-E.2    Andersson, P.G.3    Brandt, P.4
  • 41
    • 84891024145 scopus 로고    scopus 로고
    • Reduction of Carbonyl Compounds by Hydrogen Transfer
    • Andersson, P.G., Munslow, I.J., Eds.; Wiley-VCH: Weinheim, Germany
    • Gladiali, S.; Taras, R. Reduction of Carbonyl Compounds by Hydrogen Transfer. In Modern Reduction Methods; Andersson, P.G., Munslow, I.J., Eds.; Wiley-VCH: Weinheim, Germany, 2008; pp. 135-158
    • (2008) Modern Reduction Methods , pp. 135-158
    • Gladiali, S.1    Taras, R.2
  • 42
    • 84891013428 scopus 로고    scopus 로고
    • Imino Reductions by Transfer Hydrogenation
    • Andersson, P.G., Munslow, I.J., Eds.; Wiley-VCH: Weinheim, Germany
    • Wills, M. Imino Reductions by Transfer Hydrogenation. In Modern Reduction Methods; Andersson, P.G., Munslow, I.J., Eds.; Wiley-VCH: Weinheim, Germany, 2008; pp. 271-296
    • (2008) Modern Reduction Methods , pp. 271-296
    • Wills, M.1
  • 45
    • 65949096853 scopus 로고    scopus 로고
    • A novel glycerol valorization route: Chemoselective dehydrogenation catalyzed by iridium derivatives
    • Farnetti, E.; Kašpar, J.; Crotti, C. A novel glycerol valorization route: Chemoselective dehydrogenation catalyzed by iridium derivatives. Green Chem. 2009, 11, 704-709
    • (2009) Green Chem , vol.11 , pp. 704-709
    • Farnetti, E.1    Kašpar, J.2    Crotti, C.3
  • 46
    • 77954614225 scopus 로고    scopus 로고
    • Dehydrogenation of glycerol to hydroxyacetone catalyzed by iridium complexes with P-N ligands
    • Crotti, C.; Kašpar, J.; Farnetti, E. Dehydrogenation of glycerol to hydroxyacetone catalyzed by iridium complexes with P-N ligands. Green Chem. 2010, 12, 1295-1300
    • (2010) Green Chem , vol.12 , pp. 1295-1300
    • Crotti, C.1    Kašpar, J.2    Farnetti, E.3
  • 47
    • 77950202760 scopus 로고    scopus 로고
    • Tranfer hydrogenations of benzaldehyde using glycerol as solvent and hydrogen source
    • Tavor, D.; Sheviev, O.; Dlugy, C.; Wolfson, A. Tranfer hydrogenations of benzaldehyde using glycerol as solvent and hydrogen source. Can. J. Chem. 2010, 88, 305-308
    • (2010) Can. J. Chem , vol.88 , pp. 305-308
    • Tavor, D.1    Sheviev, O.2    Dlugy, C.3    Wolfson, A.4
  • 48
    • 69749100096 scopus 로고    scopus 로고
    • Glycerol as solvent and hydrogen donor in transfer hydrogenation-dehydrogenation reactions
    • Wolfson, A.; Dlugy, C.; Shotland, Y.; Tavor, D. Glycerol as solvent and hydrogen donor in transfer hydrogenation-dehydrogenation reactions. Tetrahedron Lett. 2009, 50, 5951-5953
    • (2009) Tetrahedron Lett , vol.50 , pp. 5951-5953
    • Wolfson, A.1    Dlugy, C.2    Shotland, Y.3    Tavor, D.4
  • 49
    • 80052003970 scopus 로고    scopus 로고
    • Efficient synthetic protocols in glycerol under heterogeneous conditions
    • Cravotto, G.; Orio, L.; Gaudino, E.C.; Martina, K.; Tavor, D.; Wolfson, A. Efficient synthetic protocols in glycerol under heterogeneous conditions. ChemSusChem 2011, 4, 1130-1134
    • (2011) ChemSusChem , vol.4 , pp. 1130-1134
    • Cravotto, G.1    Orio, L.2    Gaudino, E.C.3    Martina, K.4    Tavor, D.5    Wolfson, A.6
  • 50
    • 80054734460 scopus 로고    scopus 로고
    • Iridium NHC based catalysts for transfer hydrogenation processes using glycerol as solvent and hydrogen donor
    • Azua, A.; Mata, J.A.; Peris, E. Iridium NHC based catalysts for transfer hydrogenation processes using glycerol as solvent and hydrogen donor. Organometallics 2011, 30, 5532-5536
    • (2011) Organometallics , vol.30 , pp. 5532-5536
    • Azua, A.1    Mata, J.A.2    Peris, E.3
  • 51
    • 84861488404 scopus 로고    scopus 로고
    • Alternative energy input for transfer hydrogenation using iridium NHC based catalysts in glycerol as hydrogen donor and solvent
    • Azua, A.; Mata, J.A.; Peris, E.; Lamaty, F.; Martinez, J.; Colacino, E. Alternative energy input for transfer hydrogenation using iridium NHC based catalysts in glycerol as hydrogen donor and solvent. Organometallics 2012, 31, 3911-3919
    • (2012) Organometallics , vol.31 , pp. 3911-3919
    • Azua, A.1    Mata, J.A.2    Peris, E.3    Lamaty, F.4    Martinez, J.5    Colacino, E.6
  • 52
    • 84867043284 scopus 로고    scopus 로고
    • Regio-and chemoselective reduction of nitroarenes and carbonyl compounds over recyclable magnetic ferrite-nickel nanoparticles (Fe3O4-Ni) by using glycerol as a hydrogen source
    • Gawande, M.B.; Rathi, A.K.; Branco, P.S.; Nogueira, I.D.; Velhinho, A.; Shrikhande, J.J.; Indulkar, U.U.; Jayaram, R.V.; Ghumman, C.A.A.; Bundaleski, N.; et al. Regio-and chemoselective reduction of nitroarenes and carbonyl compounds over recyclable magnetic ferrite-nickel nanoparticles (Fe3O4-Ni) by using glycerol as a hydrogen source. Chem. Eur. J. 2012, 18, 12628-12632
    • (2012) Chem. Eur. J , vol.18 , pp. 12628-12632
    • Gawande, M.B.1    Rathi, A.K.2    Branco, P.S.3    Nogueira, I.D.4    Velhinho, A.5    Shrikhande, J.J.6    Indulkar, U.U.7    Jayaram, R.V.8    Ghumman, C.A.A.9    Bundaleski, N.10
  • 53
    • 79957512197 scopus 로고    scopus 로고
    • Catalytic transfer hydrogenation of olefins in glycerol
    • Tavor, D.; Popov, S.; Dlugy, C.; Wolfson, A. Catalytic transfer hydrogenation of olefins in glycerol. Org. Commun. 2010, 3, 70-75
    • (2010) Org. Commun , vol.3 , pp. 70-75
    • Tavor, D.1    Popov, S.2    Dlugy, C.3    Wolfson, A.4
  • 54
    • 79960653635 scopus 로고    scopus 로고
    • Ruthenium-catalyzed reduction of allylic alcohols using glycerol as solvent and hydrogen donor
    • Díaz-álvarez, A.E.; Crochet, P.; Cadierno, V. Ruthenium-catalyzed reduction of allylic alcohols using glycerol as solvent and hydrogen donor. Catal. Commun. 2011, 13, 91-96
    • (2011) Catal. Commun , vol.13 , pp. 91-96
    • Díaz-álvarez, A.E.1    Crochet, P.2    Cadierno, V.3
  • 55
    • 34250220349 scopus 로고    scopus 로고
    • Ruthenium-catalyzed reduction of allylic alcohols: An efficient isomerization/transfer hydrogenation tandem process
    • Cadierno, V.; Francos, J.; Gimeno, J.; Nebra, N. Ruthenium-catalyzed reduction of allylic alcohols: An efficient isomerization/transfer hydrogenation tandem process. Chem. Commun. 2007, 2536-2538
    • (2007) Chem. Commun , pp. 2536-2538
    • Cadierno, V.1    Francos, J.2    Gimeno, J.3    Nebra, N.4
  • 56
    • 71549139771 scopus 로고    scopus 로고
    • Ruthenium-catalyzed isomerization/transfer hydrogenation in organic and aqueous media: A one-pot tandem process for the reduction of allylic alcohols
    • Cadierno, V.; Crochet, P.; Francos, J.; García-Garrido, S.E.; Gimeno, J.; Nebra, N. Ruthenium-catalyzed isomerization/transfer hydrogenation in organic and aqueous media: A one-pot tandem process for the reduction of allylic alcohols. Green Chem. 2009, 11, 1992-2000
    • (2009) Green Chem , vol.11 , pp. 1992-2000
    • Cadierno, V.1    Crochet, P.2    Francos, J.3    García-Garrido, S.E.4    Gimeno, J.5    Nebra, N.6
  • 58
    • 79960909240 scopus 로고    scopus 로고
    • Transfer hydrogenations of nitrobenzene using glycerol as solvent and hydrogen donor
    • Tavor, D.; Gefen, I.; Dlugy, C.; Wolfson, A. Transfer hydrogenations of nitrobenzene using glycerol as solvent and hydrogen donor. Synth. Commun. 2011, 41, 3409-3416
    • (2011) Synth. Commun , vol.41 , pp. 3409-3416
    • Tavor, D.1    Gefen, I.2    Dlugy, C.3    Wolfson, A.4
  • 60
    • 80052956616 scopus 로고    scopus 로고
    • RuII-mediated hydrogen transfer from aqueous glycerol to CO2: From waste to value-added products
    • Dibenedetto, A.; Stufano, P.; Nocito, F.; Aresta, M. RuII-mediated hydrogen transfer from aqueous glycerol to CO2: From waste to value-added products. ChemSusChem 2011, 4, 1311-1315
    • (2011) ChemSusChem , vol.4 , pp. 1311-1315
    • Dibenedetto, A.1    Stufano, P.2    Nocito, F.3    Aresta, M.4
  • 61
    • 77954274202 scopus 로고    scopus 로고
    • "(6-arene)Ru(bis-NHC)" complexes for the reduction of CO2 to formate with hydrogen and by transfer hydrogenation with iPrOH
    • Sanz, A.; Azua, A.; Peris, E. "(6-arene)Ru(bis-NHC)" complexes for the reduction of CO2 to formate with hydrogen and by transfer hydrogenation with iPrOH. Organometallics 2010, 39, 6339-6343
    • (2010) Organometallics , vol.39 , pp. 6339-6343
    • Sanz, A.1    Azua, A.2    Peris, E.3
  • 62
    • 84875579076 scopus 로고    scopus 로고
    • Heterogeneously catalysed mild hydrogenolytic depolymerisation of lignin under microwave irradiation with hydrogen-donating solvents
    • Toledano, A.; Serrano, L.; Labidi, J.; Pineda, A.; Balu, A.M.; Luque, R. Heterogeneously catalysed mild hydrogenolytic depolymerisation of lignin under microwave irradiation with hydrogen-donating solvents. ChemCatChem 2012, doi:10.1002/cctc.201200616
    • (2012) ChemCatChem
    • Toledano, A.1    Serrano, L.2    Labidi, J.3    Pineda, A.4    Balu, A.M.5    Luque, R.6
  • 63
    • 79951536561 scopus 로고    scopus 로고
    • Preparation of elemental Cu and Ni nanoparticles by the polyol method: An experimental and theoretical approach
    • and references cited therein
    • Carroll, K.J.; Reveles, J.U.; Shultz, M.D.; Khanna, S.N.; Carpenter, E.E. Preparation of elemental Cu and Ni nanoparticles by the polyol method: An experimental and theoretical approach. J. Phys. Chem. C 2011, 115, 2656-2664 and references cited therein
    • (2011) J. Phys. Chem. C , vol.115 , pp. 2656-2664
    • Carroll, K.J.1    Reveles, J.U.2    Shultz, M.D.3    Khanna, S.N.4    Carpenter, E.E.5
  • 64
    • 1542533797 scopus 로고    scopus 로고
    • Reduction and aggregation of silver and thallium ions in viscous media
    • Rele, M.; Kapoor, S.; Sharma, G.; Mukherjee, T. Reduction and aggregation of silver and thallium ions in viscous media. Phys. Chem. Chem. Phys. 2004, 6, 590-595
    • (2004) Phys. Chem. Chem. Phys , vol.6 , pp. 590-595
    • Rele, M.1    Kapoor, S.2    Sharma, G.3    Mukherjee, T.4
  • 65
    • 33645987001 scopus 로고    scopus 로고
    • In-situ preparation of binary-phase silver nanoparticles at a high Ag+ concentration
    • Ullah, M.H.; Kim, I.; Ha, C.-S. In-situ preparation of binary-phase silver nanoparticles at a high Ag+ concentration. J. Nanosci. Nanotechnol. 2006, 6, 777-782
    • (2006) J. Nanosci. Nanotechnol , vol.6 , pp. 777-782
    • Ullah, M.H.1    Kim, I.2    Ha, C.-S.3
  • 66
    • 33644869516 scopus 로고    scopus 로고
    • Preparation and optical properties of silver nanoparticles at a high Ag+ concentration
    • Ullah, M.H.; Kim, I.; Ha, C.-S. Preparation and optical properties of silver nanoparticles at a high Ag+ concentration. Mater. Lett. 2006, 60, 1496-1501
    • (2006) Mater. Lett , vol.60 , pp. 1496-1501
    • Ullah, M.H.1    Kim, I.2    Ha, C.-S.3
  • 67
    • 34249787584 scopus 로고    scopus 로고
    • One pot synthesis of polymer protected Pt, Pd, Ag and Ru nanoparticles and nanoprisms under reflux and microwave mode of heating in glycerol-A comparative study
    • Grace, A.N.; Pandian, K. One pot synthesis of polymer protected Pt, Pd, Ag and Ru nanoparticles and nanoprisms under reflux and microwave mode of heating in glycerol-A comparative study. Mat. Chem. Phys. 2007, 104, 191-198
    • (2007) Mat. Chem. Phys , vol.104 , pp. 191-198
    • Grace, A.N.1    Pandian, K.2
  • 68
    • 77955853579 scopus 로고    scopus 로고
    • Synthesis and characterization of silver nanoparticles in viscous solvents and its transfer into non-polar solvents
    • Sarkar, A.; Kapoor, S.; Mukherjee, T. Synthesis and characterization of silver nanoparticles in viscous solvents and its transfer into non-polar solvents. Res. Chem. Intermed. 2010, 36, 411-421
    • (2010) Res. Chem. Intermed , vol.36 , pp. 411-421
    • Sarkar, A.1    Kapoor, S.2    Mukherjee, T.3
  • 69
    • 80052590633 scopus 로고    scopus 로고
    • Fabrication of silver nanoparticles in a continuous flow, low temperature microwave-assisted polyol process
    • Dzido, G.; Jarzebski, A.B. Fabrication of silver nanoparticles in a continuous flow, low temperature microwave-assisted polyol process. J. Nanopart. Res. 2011, 13, 2533-2541
    • (2011) J. Nanopart. Res , vol.13 , pp. 2533-2541
    • Dzido, G.1    Jarzebski, A.B.2
  • 70
    • 80052566347 scopus 로고    scopus 로고
    • Fabrication of silver hollow microspheres by sodium hydroxide in glycerol solution
    • Preuksarattanawut, T.; Asavavisithchai, S.; Nisaratanoporn, E. Fabrication of silver hollow microspheres by sodium hydroxide in glycerol solution. Mat. Chem. Phys. 2011, 130, 481-486
    • (2011) Mat. Chem. Phys , vol.130 , pp. 481-486
    • Preuksarattanawut, T.1    Asavavisithchai, S.2    Nisaratanoporn, E.3
  • 71
    • 84864453617 scopus 로고    scopus 로고
    • Straightforward synthesis of carbon-supported Ag nanoparticles and their application for the oxygen reduction reaction
    • Garcia, A.C.; Gasparotto, L.H.S.; Gomes, J.F.; Tremiliosi-Filho, G. Straightforward synthesis of carbon-supported Ag nanoparticles and their application for the oxygen reduction reaction. Electrocatalysis 2012, 3, 147-152
    • (2012) Electrocatalysis , vol.3 , pp. 147-152
    • Garcia, A.C.1    Gasparotto, L.H.S.2    Gomes, J.F.3    Tremiliosi-Filho, G.4
  • 72
    • 80053343995 scopus 로고    scopus 로고
    • Glycerol-mediated synthesis of Pd nanostructures with dominant (111) facets for enhanced electrocatalytic activity
    • Lee, Y.-W.; Han, S.-B.; Ko, A.R.; Kim, H.-S.; Park, K.-W. Glycerol-mediated synthesis of Pd nanostructures with dominant (111) facets for enhanced electrocatalytic activity. Catal. Commun. 2011, 15, 137-140
    • (2011) Catal. Commun , vol.15 , pp. 137-140
    • Lee, Y.-W.1    Han, S.-B.2    Ko, A.R.3    Kim, H.-S.4    Park, K.-W.5
  • 73
    • 84866445539 scopus 로고    scopus 로고
    • Electrochemical oxidation of some basic alcohols on multiwalled carbon nanotube-platinum composites
    • Koo, M.; Bae, J.-S.; Kim, H.-C.; Nam, D.-G.; Ko, C.H.; Yeum, J.H.; Oh, W. Electrochemical oxidation of some basic alcohols on multiwalled carbon nanotube-platinum composites. Bull. Mater. Sci. 2012, 35, 545-550
    • (2012) Bull. Mater. Sci , vol.35 , pp. 545-550
    • Koo, M.1    Bae, J.-S.2    Kim, H.-C.3    Nam, D.-G.4    Ko, C.H.5    Yeum, J.H.6    Oh, W.7
  • 74
    • 43049183425 scopus 로고    scopus 로고
    • Electrocatalytic oxidation of ethylene glycol on Pt and Pt-Ru nanoparticles modified multi-walled carbon nanotubes
    • Selvaraj, V.; Vinoba, M.; Alagar, M. Electrocatalytic oxidation of ethylene glycol on Pt and Pt-Ru nanoparticles modified multi-walled carbon nanotubes. J. Colloid Interf. Sci. 2008, 322, 537-544
    • (2008) J. Colloid Interf. Sci , vol.322 , pp. 537-544
    • Selvaraj, V.1    Vinoba, M.2    Alagar, M.3
  • 75
    • 84864808155 scopus 로고    scopus 로고
    • Electrocatalytic performances of environmentally friendly synthesized gold nanoparticles towards the borohydride electro-oxidation reaction
    • Gasparotto, L.H.S.; Garcia, A.C.; Gomes, J.F.; Tremiliosi-Filho, G. Electrocatalytic performances of environmentally friendly synthesized gold nanoparticles towards the borohydride electro-oxidation reaction. J. Power Sources 2012, 218, 73-78
    • (2012) J. Power Sources , vol.218 , pp. 73-78
    • Gasparotto, L.H.S.1    Garcia, A.C.2    Gomes, J.F.3    Tremiliosi-Filho, G.4
  • 76
    • 84861183290 scopus 로고    scopus 로고
    • Highly active Pt-Pd alloy catalyst for oxygen reduction reaction in buffer solution
    • Lee, Y.-W.; Oh, S.-E.; Park, K.-W. Highly active Pt-Pd alloy catalyst for oxygen reduction reaction in buffer solution. Electrochem. Commun. 2011, 13, 1300-1303
    • (2011) Electrochem. Commun , vol.13 , pp. 1300-1303
    • Lee, Y.-W.1    Oh, S.-E.2    Park, K.-W.3
  • 77
    • 79952718141 scopus 로고    scopus 로고
    • Synthesis of octahedral Pt-Pd alloy nanoparticles for improved catalytic activity and stability in methanol electrooxidation
    • Lee, Y.-W.; Ko, A.-R.; Han, S.-B.; Kim, H.-S.; Park, K.-W. Synthesis of octahedral Pt-Pd alloy nanoparticles for improved catalytic activity and stability in methanol electrooxidation. Phys. Chem. Chem. Phys. 2011, 13, 5569-5572
    • (2011) Phys. Chem. Chem. Phys , vol.13 , pp. 5569-5572
    • Lee, Y.-W.1    Ko, A.-R.2    Han, S.-B.3    Kim, H.-S.4    Park, K.-W.5
  • 78
    • 84859207523 scopus 로고    scopus 로고
    • Octahedral Pt-Pd alloy catalysts with enhanced oxygen reduction activity and stability in proton exchange membrane fuel cells
    • Lee, Y.-W.; Ko, A.-R.; Kim, D.-Y.; Han, S.-B.; Park, K.-W. Octahedral Pt-Pd alloy catalysts with enhanced oxygen reduction activity and stability in proton exchange membrane fuel cells. RSC Adv. 2012, 2, 1119-1125
    • (2012) RSC Adv , vol.2 , pp. 1119-1125
    • Lee, Y.-W.1    Ko, A.-R.2    Kim, D.-Y.3    Han, S.-B.4    Park, K.-W.5
  • 79
    • 84870953612 scopus 로고    scopus 로고
    • Preparation of CoSe nanoparticles by microwave-assisted polyol method: Effect of Se/Co ratio, support type and synthesis conditions on oxygen reduction activity
    • Nekooi, P.; Ahmadi, R.; Amini, M.K. Preparation of CoSe nanoparticles by microwave-assisted polyol method: Effect of Se/Co ratio, support type and synthesis conditions on oxygen reduction activity. J. Iran Chem. Soc. 2012, 9, 715-722
    • (2012) J. Iran Chem. Soc , vol.9 , pp. 715-722
    • Nekooi, P.1    Ahmadi, R.2    Amini, M.K.3
  • 80
    • 0043011744 scopus 로고    scopus 로고
    • Hydrothermal reduction route to Mn(OH)2 and MnCO3 nanocrystals
    • Wang, X.; Li, Y. Hydrothermal reduction route to Mn(OH)2 and MnCO3 nanocrystals. Mat. Chem. Phys. 2003, 82, 419-422
    • (2003) Mat. Chem. Phys , vol.82 , pp. 419-422
    • Wang, X.1    Li, Y.2
  • 81
    • 80055057799 scopus 로고    scopus 로고
    • Preparation of VO2(B) nanoflake with glycerol as reductant agent and its catalytic application in the aerobic oxidation of benzene to phenol
    • Chen, X.; Wang, F.; Xu, J. Preparation of VO2(B) nanoflake with glycerol as reductant agent and its catalytic application in the aerobic oxidation of benzene to phenol. Top. Catal. 2011, 54, 1016-1023
    • (2011) Top. Catal , vol.54 , pp. 1016-1023
    • Chen, X.1    Wang, F.2    Xu, J.3
  • 82
    • 84871800257 scopus 로고    scopus 로고
    • Speedy fabrication of diameter-controlled Ag nanowires using glycerol under microwave irradiation conditions
    • Kou, J.; Varma, R.S. Speedy fabrication of diameter-controlled Ag nanowires using glycerol under microwave irradiation conditions. Chem. Commun. 2013, 49, 692-694
    • (2013) Chem. Commun , vol.49 , pp. 692-694
    • Kou, J.1    Varma, R.S.2


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