Triflic Acid-Functionalized Silica-Coated Magnetic Nanoparticles as a Magnetically Separable Catalyst for Synthesis of gem-Dihydroperoxides

Triflic acid‐functionalized silica‐coated magnetic nanoparticles [γ‐Fe2O3@SiO2‐TfOH] were readily prepared and identified as an effictive catalyst for the transformation of aldehydes or ketones into their corresponding gem‐dihydroperoxides with 30% aqueous hydrogen peroxide. The catalyst was easily...

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Published inAdvanced synthesis & catalysis Vol. 354; no. 2-3; pp. 441 - 447
Main Authors Liu, Yong-Hui, Deng, Jia, Gao, Jian-Wu, Zhang, Zhan-Hui
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.02.2012
WILEY‐VCH Verlag
Wiley
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ISSN1615-4150
1615-4169
DOI10.1002/adsc.201100561

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Abstract Triflic acid‐functionalized silica‐coated magnetic nanoparticles [γ‐Fe2O3@SiO2‐TfOH] were readily prepared and identified as an effictive catalyst for the transformation of aldehydes or ketones into their corresponding gem‐dihydroperoxides with 30% aqueous hydrogen peroxide. The catalyst was easily separated by magnetic decantation and the recovered catalyst was reused for seven cycles without significant loss of catalytic activity.
AbstractList Triflic acid‐functionalized silica‐coated magnetic nanoparticles [γ‐Fe 2 O 3 @SiO 2 ‐TfOH] were readily prepared and identified as an effictive catalyst for the transformation of aldehydes or ketones into their corresponding gem ‐dihydroperoxides with 30% aqueous hydrogen peroxide. The catalyst was easily separated by magnetic decantation and the recovered catalyst was reused for seven cycles without significant loss of catalytic activity.
Triflic acid‐functionalized silica‐coated magnetic nanoparticles [γ‐Fe2O3@SiO2‐TfOH] were readily prepared and identified as an effictive catalyst for the transformation of aldehydes or ketones into their corresponding gem‐dihydroperoxides with 30% aqueous hydrogen peroxide. The catalyst was easily separated by magnetic decantation and the recovered catalyst was reused for seven cycles without significant loss of catalytic activity.
Triflic acid-functionalized silica-coated magnetic nanoparticles [?-Fe2O3@SiO2-TfOH] were readily prepared and identified as an effictive catalyst for the transformation of aldehydes or ketones into their corresponding gem-dihydroperoxides with 30% aqueous hydrogen peroxide. The catalyst was easily separated by magnetic decantation and the recovered catalyst was reused for seven cycles without significant loss of catalytic activity.
Author Liu, Yong-Hui
Deng, Jia
Gao, Jian-Wu
Zhang, Zhan-Hui
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  fullname: Deng, Jia
  organization: Key Laboratory of Inorganic Nanomaterial of Hebei Province, College of Chemistry & Material Science, Hebei Normal University, Shijiazhuang 050024, People's Republic of China, Fax: (+86)-311-8963-2795
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  givenname: Jian-Wu
  surname: Gao
  fullname: Gao, Jian-Wu
  organization: Key Laboratory of Inorganic Nanomaterial of Hebei Province, College of Chemistry & Material Science, Hebei Normal University, Shijiazhuang 050024, People's Republic of China, Fax: (+86)-311-8963-2795
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  organization: Key Laboratory of Inorganic Nanomaterial of Hebei Province, College of Chemistry & Material Science, Hebei Normal University, Shijiazhuang 050024, People's Republic of China, Fax: (+86)-311-8963-2795
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Issue 2-3
Keywords magnetic catalysts
FE3O4 NANOPARTICLES
AQUEOUS HYDROGEN-PEROXIDE
GEMINAL BISHYDROPEROXIDES
EFFICIENT SYNTHESIS
CARBONYL-COMPOUNDS
gem-dihydroperoxides
HETEROGENEOUS CATALYSIS
ketones
LIGHT IRRADIATION
aldehydes
functionalized silica-coated magnetic nanoparticles
ANTIMALARIAL ACTIVITY
RECYCLABLE CATALYST
MOLECULAR-OXYGEN
Hydrogen peroxide
Nanoparticle
Reuse
Trifluoromethanesulfonic acid
Aldehyde
Ketone
Silica
Magnetic particles
Functionalization
Magnetic separation
Aqueous solution
Iron III Oxides
Chemical synthesis
Catalyst activity
Catalyst
Maghemite
Organic peroxide
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2010; 16
2010; 15
2010 2010; 122 49
2004; 24
2011; 52
2003; 59
2010; 384
2011; 13
2007; 72
2009; 351
2001; 44
2010; 63
2011; 111
2011; 353
2007; 37
2009; 11
2010; 24
2001
2000
2009; 50
2002; 45
2010; 352
1996; 61
2011; 67
2007; 5
2010; 2
2010; 5
2011
2010
2009
2006; 8
2008
2011; 76
2008; 10
2008; 51
2008; 284
2010; 44
1990; 20
2004; 53
2003 2003; 115 42
2010; 46
2008; 49
2006; 47
2010; 377
2005; 5
2010; 254
2009; 9
2007 2007; 119 46
2006; 348
2008; 296
2007; 48
e_1_2_6_51_2
e_1_2_6_72_2
e_1_2_6_53_2
e_1_2_6_74_2
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e_1_2_6_30_2
e_1_2_6_70_2
e_1_2_6_19_2
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e_1_2_6_9_3
e_1_2_6_9_2
e_1_2_6_3_2
e_1_2_6_5_2
Zeng T. Q. (e_1_2_6_25_2) 2010
e_1_2_6_24_2
e_1_2_6_47_2
e_1_2_6_22_2
e_1_2_6_49_2
e_1_2_6_1_2
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e_1_2_6_52_2
e_1_2_6_75_2
e_1_2_6_71_2
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Cano R. (e_1_2_6_31_2) 2011
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e_1_2_6_12_2
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e_1_2_6_86_3
e_1_2_6_67_2
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Ma'mani, L (WOS:000276419000009) 2010; 377
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Shylesh, S. (000300448400024.53) 2010; 122
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Zmitek, K (WOS:000251274700002) 2007; 5
Bunge, A (WOS:000267901800015) 2009; 50
Zeng, TQ (WOS:000276973200003) 2010; 12
Zhang, ZH (WOS:000234964700021) 2006; 348
Liu, YH (WOS:000261538500006) 2008; 296
Wang, HJ (WOS:000288183000013) 2011; 13
Cano, R (WOS:000292480300005) 2011; 76
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Ito, T (WOS:000180645800010) 2003; 59
JEFFORD, CW (WOS:A1990EL86300005) 1990; 20
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Zeng, TQ (WOS:000286577600024) 2011; 13
Cano, R (WOS:000294161400013) 2011
Zhang, ZH (WOS:000281629900007) 2010; 12
Ramirez, AP (WOS:000262913500003) 2009; 11
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Liu, YH (WOS:000263383400018) 2009; 50
Mori, K (WOS:000269493700008) 2009; 11
Megia-Fernandez, A (WOS:000285397800032) 2010; 352
Lu, HY (WOS:000280727900022) 2010; 63
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Terent'ev, AO (WOS:000247620500026) 2007; 37
Shylesh, S (WOS:000275235800025) 2010; 352
Das, B (WOS:000249216800011) 2007; 48
Liu, GH (WOS:000291530800019) 2011; 353
Shylesh, S (WOS:000277782200004) 2010; 49
Polshettiwar, V (WOS:000290373100002) 2011; 111
Firouzabadi, H (WOS:000287103200016) 2011; 353
Cano, R (WOS:000292573700010) 2011; 67
Zmitek, K (WOS:000248793400026) 2007; 72
Amali, AJ (WOS:000271476500013) 2009; 11
Li, Y (WOS:000264622600054) 2009; 11
Zhu, YH (WOS:000277207800001) 2010; 2
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Tang, YQ (WOS:000222199300002) 2004; 24
Shylesh, S (WOS:000269583900015) 2009; 351
Terent'ev, A. O. (000300448400024.60) 2004; 53
Azarifar, D (WOS:000275956900027) 2010; 15
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SSID ssj0017877
Score 2.388669
Snippet Triflic acid‐functionalized silica‐coated magnetic nanoparticles [γ‐Fe2O3@SiO2‐TfOH] were readily prepared and identified as an effictive catalyst for the...
Triflic acid‐functionalized silica‐coated magnetic nanoparticles [γ‐Fe 2 O 3 @SiO 2 ‐TfOH] were readily prepared and identified as an effictive catalyst for...
Triflic acid-functionalized silica-coated magnetic nanoparticles [?-Fe2O3@SiO2-TfOH] were readily prepared and identified as an effictive catalyst for the...
Source Web of Science
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webofscience
crossref
wiley
istex
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StartPage 441
SubjectTerms aldehydes
Aliphatic compounds
Catalysis
Catalysts: preparations and properties
Chemistry
Chemistry, Applied
Chemistry, Organic
Exact sciences and technology
functionalized silica-coated magnetic nanoparticles
gem-dihydroperoxides
General and physical chemistry
ketones
magnetic catalysts
Organic chemistry
Physical Sciences
Preparations and properties
Science & Technology
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
Title Triflic Acid-Functionalized Silica-Coated Magnetic Nanoparticles as a Magnetically Separable Catalyst for Synthesis of gem-Dihydroperoxides
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https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fadsc.201100561
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Volume 354
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