Abstract
An efficient magnetic nanocomposite catalyst (Fe3O4@GO) was synthesized and utilized as a sustainable and convenient catalyst for Baeyer–Villiger oxidation. The catalyst was characterized by XRD, FT-IR, TEM, SEM, XPS, Raman and VSM. Under solvent free conditions, hydrogen peroxide as green oxidant, Fe3O4@GO showed an efficient catalytic activity and excellent selectivity for Baeyer–Villiger oxidation at room temperature. Conversion of 2-methyl cyclohexanone and selectivity of ε-heptanlactone were 84% and 94%, respectively. The catalyst can be magnetically reused and recycled for several runs without any significant loss in efficiency and selectivity.
Graphical Abstract
An efficient magnetic nanocomposite catalyst (Fe3O4@GO) was synthesized to show high catalytic activity and excellent selectivity for the Baeyer–Villiger oxidation under solvent free conditions with hydrogen peroxide.
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References
Liu Y, Li Z, Shen W (2008) Recent Pat Chem Eng 1:1
Toebes ML, Prinsloo FF, Bitter JH (2003) J Catal 214:78
Kuila T, Mishra AK, Khanra P (2013) Nanoscale 5:52
Gao W (2015) Springer International Publishing, pp 61–95
Marcano DC, Kosynkin DV, Berlin JM (2010) ACS Nano 4:4806
Dreyer DR, Park S, Bielawski CW (2009) Chem Soc Rev 39:228
Zhu Y, Murali S, Cai W (2010) Cheminform 22:3906
Chen D, Feng H, Li J (2012) Chem Rev 112:6027
Dikin DA, Stankovich S, Zimney EJ (2015) Nature 448:457
Dhakshinamoorthy A, Alvaro M, Garcia H (2012) Chem Commun 48:11275
Yang S, Zhang ZH, Chen Q (2017) Appl Organomet Chem e4132. https://doi.org/10.1002/aoc.4132
Pescarmona PP, Jacobs PA (2008) Catal Today 137:52
Haag DR, Kung HH (2014) Top Catal 57:764
Wiltshire JG, Li LJ, Khlobystov AN (2005) Carbon 43:1151
Arash GC, Darvishnejad Z, Norouzi M (2015) Appl Organomet Chem 29:170
Krow GR (1993) Org React 43:251
Strukul G (2010) Cheminform 29:31
Ech JP, Carretero MA (2017) Chemcatchem 9:15
Fischer J, Holderich WF (1999) Appl Catal A 180:435
Schreiber SL, Liew WF (1983) Tetrahedron Lett 24:2363
Cesar JS, Jose RR (2011) Tetrahedron 2008:64
Benito A, Moustafa FA, Miguel AS (1995) Tetrahedron Lett 36:3401
Corma A, Navarro MT, Renz M (2003) J Catal 219:242
Lei Z, Zhang Q, Wang R (2006) ChemInform 691:5767
Pillai UR, Sahle-Demessie E (2003) J Mol Catal A 191:93
Zhou XT, Ji HB, Yuan QL (2009) J Porphyr Phthalocyanines 12:94
Lei ZQ, Wei LL, Wang RR (2008) Catal Commun 9:15
Ma Y, Liang Z, Feng S (2015) Appl Organomet Chem 29:7
Olszówka JE, Karcz R, Napruszewska BD (2018) Catal Commun 107:48–52
Guan FF, Ma TT, Yuan X (2018) Catal Lett 148:443
Modi CK, Solanki N, Vithalani R (2017) Appl Organomet Chem 32:e3910
Cuetos A, Rioz-Martínez A, Valenzuela ML (2012) J Mol Catal B 74:178
Torres Pazmiño DE, Dudek HM, Fraaije MW (2010) Curr Opin Chem Biol 14:138
Du GH, Liu ZL, Xia X, Chu Q, Zhang SM (2006) J Sol-Gel Sci Technol 39:285
Huo X, Liu J, Wang B, Zhang H, Yang Z, She X, Xi P (2013) J Mater Chem A 1:651
Corma A, Renz M (2004) Chem Commun 35:550
Aunkor MTH, Mahbubul IM, Saidurb R, Metselaar HSC (2016) RSC Adv 6:27807
Li P, Jiang EY, Bai HL (2011) J Phys D 44:7879
Hara T, Hatakeyama M, Kim A, Ichikuni N, Shimazu S (2012) Green Chem 14:771
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Xiao, G., Gao, X., Yan, W. et al. Baeyer–Villiger Oxidation of Cyclohexanone by Hydrogen Peroxide with Fe3O4@GO as Catalyst Under Solvent Free Conditions. Catal Lett 149, 1765–1771 (2019). https://doi.org/10.1007/s10562-019-02765-z
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DOI: https://doi.org/10.1007/s10562-019-02765-z