Nano-Polyoxotungstate as a Recyclable and Highly Efficient Catalyst for Cycloaddition of CO2 to Cyclic Carbonates under Solvent-Free Conditions

被引:3
作者
Haddad, Reza [1 ]
Telgerd, Mehdi D. [2 ]
Abedi, Hamid [1 ]
Roostaie, Ali [1 ]
机构
[1] Police Sci & Social Studies Inst, Technol Management Dept, Tehran 193956516, Iran
[2] Univ Tehran Med Sci, Pharmaceut Biomat Dept, Tehran, Iran
关键词
Coupling reaction; green chemistry; CO2; magnetic nano-particles; cyclic carbonate; keplerate polyoxometalates; CHEMICAL FIXATION; PROPYLENE CARBONATE; COUPLING REACTIONS; HETEROGENEOUS CATALYST; GRAPHENE OXIDE; WATER-TOLERANT; IONIC LIQUID; EPOXIDES; DIOXIDE; POLYOXOMETALATE;
D O I
10.2174/1570179414666170614122804
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Aim and Objective: In this study, for the first time keplerate cluster [Cu20Cl(OH)(24)(H2O)(12 )(P8W48O184)](25-) (hereafter [W48P8Cu20]) was supported on SMNP (Fe3O4-@SiO2) via amine functionality (ASMNP) as a magnetically-recoverable catalyst (hereafter [WPCu@ASMNP]). This nanocatalyst showed high activity for the synthesis of cyclic carbonates under solvent-free conditions. Materials and Methods: After preparation, the nanocatalyst was characterized by FT-IR, XRD, ICP-AES, TGA, TEM and SEM. Surface acidity was determined by a potentiometric titration with n-butyl amine. The effect of different parameters like catalyst amount, reaction time, temperature and pressure in the presence of [WPCu@ASMNP] were studied. Results: Optimal reaction conditions were obtained for 0.5mol% of catalyst, reaction temperature of 100 degrees C and CO2 pressure of 1.5 MPa. The [WPCu@ASMNP] could be separated from the reaction and reused for five times with an external magnet without notable decrease in the activity. Finally, stability of the catalyst and its reusability were evaluated using a hot filtration method. The FT-IR and the control experiments (hot filtration) after five cycles confirmed the strongly catalyst immobilization to the ASMNP. Conclusion: The nanocatalyst is shown to be effective heterogeneous and recyclable catalyst for the synthesis of cyclic carbonates from CO2 and epoxides under mild conditions without any additional co-solvent and cocatalyst. This catalyst has a good substrate tolerance as demonstrated by its activity towards different epoxides. Importantly, the reaction could be carried out under solvent free conditions. The heterogeneous nature of the catalyst is proved by recovering and reusing this catalyst without any appreciable loss in catalytic activity and by the FT-IR spectroscopic characterization of the fresh and spent catalyst. The product separation and catalyst recycling are short using an external magnet.
引用
收藏
页码:533 / 540
页数:8
相关论文
共 84 条
[1]   ACTIVATION OF CARBON-DIOXIDE WITH ALUMINUM PORPHYRIN AND REACTION WITH EPOXIDE - STUDIES ON (TETRAPHENYLPORPHINATO)ALUMINUM ALKOXIDE HAVING A LONG OXYALKYLENE CHAIN AS THE ALKOXIDE GROUP [J].
AIDA, T ;
INOUE, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (05) :1304-1309
[2]   High-activity, single-site catalysts for the alternating copolymerization of CO2 and propylene oxide [J].
Allen, SD ;
Moore, DR ;
Lobkovsky, EB ;
Coates, GW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (48) :14284-14285
[3]   CO2 fixation using recoverable chromium salen catalysts:: use of ionic liquids as cosolvent or high-surface-area silicates as supports [J].
Alvaro, M ;
Baleizao, C ;
Das, D ;
Carbonell, E ;
García, H .
JOURNAL OF CATALYSIS, 2004, 228 (01) :254-258
[4]   Meeting the challenges to sustainability through green chemistry [J].
Anastas, PT .
GREEN CHEMISTRY, 2003, 5 (02) :G29-G34
[5]  
[Anonymous], 2013, GREEN CHEM, V15, P1173
[6]  
[Anonymous], CHEM SOC REV
[7]   Catalysis research of relevance to carbon management: Progress, challenges, and opportunities [J].
Arakawa, H ;
Aresta, M ;
Armor, JN ;
Barteau, MA ;
Beckman, EJ ;
Bell, AT ;
Bercaw, JE ;
Creutz, C ;
Dinjus, E ;
Dixon, DA ;
Domen, K ;
DuBois, DL ;
Eckert, J ;
Fujita, E ;
Gibson, DH ;
Goddard, WA ;
Goodman, DW ;
Keller, J ;
Kubas, GJ ;
Kung, HH ;
Lyons, JE ;
Manzer, LE ;
Marks, TJ ;
Morokuma, K ;
Nicholas, KM ;
Periana, R ;
Que, L ;
Rostrup-Nielson, J ;
Sachtler, WMH ;
Schmidt, LD ;
Sen, A ;
Somorjai, GA ;
Stair, PC ;
Stults, BR ;
Tumas, W .
CHEMICAL REVIEWS, 2001, 101 (04) :953-996
[8]   Carbon Dioxide Fixation by Cycloaddition with Epoxides, Catalyzed by Biomimetic Metalloporphyrins [J].
Bai, Dongsheng ;
Duan, Shuhui ;
Hai, Long ;
Jing, Huanwang .
CHEMCATCHEM, 2012, 4 (11) :1752-1758
[9]   Cycloaddition of CO2 to epoxides over both homogeneous and silica-supported guanidine catalysts [J].
Barbarini, A ;
Maggi, R ;
Mazzacani, A ;
Mori, G ;
Sartori, G ;
Sartorio, R .
TETRAHEDRON LETTERS, 2003, 44 (14) :2931-2934
[10]   Propylene carbonate as a solvent for asymmetric Hydrogenations [J].
Bayardon, Jerome ;
Holz, Jens ;
Schaeffner, Benjamin ;
Andrushko, Vasyl ;
Verevkin, Sergej ;
Preetz, Angelika ;
Boerner, Armin .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (31) :5971-5974