Formation and decomposition of N,N,N-trimethylanilinium cations on zeolite H-Y investigated by in situ stopped-flow MAS NMR spectroscopy

被引:26
作者
Wang, W
Seiler, M
Ivanova, II
Sternberg, U
Weitkamp, J
Hunger, M
机构
[1] Univ Jena, Fac Phys & Astron, D-07743 Jena, Germany
[2] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119899, Russia
[3] Univ Stuttgart, Inst Chem Technol, D-70550 Stuttgart, Germany
关键词
D O I
10.1021/ja012675n
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Methylation of aniline by methanol on zeolite H-Y has been investigated by in situ C-13 MAS NMR spectroscopy under flow conditions. The in Situ 13C continuous-flow (CF) MAS NMR experiments were performed at reaction temperatures between 473 and 523 K, molar methanol-to-aniline ratios of 1:1 to 4:1, and modified residence times of (CH3OH)-C-13 between 20 and 100 (g.h)/mol. The methylation reaction was shown to start at 473 K. N,N,N-Trimethylanilinium cations causing a 13C NMR signal at 58 ppm constitute the major product on the catalyst surface. Small amounts of protonated N-methylaniline ([PhNH2CH3](+)) and N,N-dimethylaniline ([PhNH(CH3)(2)](+)) were also observed at ca. 39 and 48 ppm, respectively. After increase of the temperature to 523 K, the contents of N,N-dimethylanilinium cations and ring-alkylated reaction products strongly increased, accompanied by a decrease of the amount of N,N,N-trimethylanilinium cations. With application of the in situ stopped-flow (SF) MAS NMR technique, the decomposition of N,N,N-trimethylanilinium cations on zeolite H-Y to N,N-dimethylanilinium and N-methylanilinium cations was investigated to gain a deeper insight into the reaction mechanism. The results obtained allow the proposal of a mechanism consisting of three steps: (i) the conversion of methanol to surface methoxy groups and dimethyl ether (DME); (d) the alkylation of aniline with methanol, methoxy groups, or DME leading to an equilibrium mixture of N,N,N-trimethylanilinium, N,N-dimethylanilinium, and N-methylanilinium cations attached to the zeolite surface; (iii) the deprotonation of NN-dimethylanilinium and N-methylanilinium cations causing the formation of N,N-dimethylaniline (NNDMA) and N-methylaniline (NMA) in the gas phase, respectively. The chemical equilibrium between the anilinium cations carrying different numbers of methyl groups is suggested to play a key role for the products distribution in the gas phase.
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页码:7548 / 7554
页数:7
相关论文
共 61 条
[1]   Carbon and nitrogen basicity of aminothiophenes and anilines [J].
Bagno, A ;
Terrier, F .
JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (26) :6537-6542
[2]   Formation of N-methylaniline by transalkylation of aniline with N,N-dimethylaniline over zeolite Beta [J].
Bandyopadhyay, R ;
Singh, PS ;
Rao, BS .
APPLIED CATALYSIS A-GENERAL, 1997, 155 (01) :27-39
[3]   N-alkylation of aniline with methanol over CrPO4 and CrPO4-AlPO4 (5-50 wt% AlPO4) catalysts [J].
Bautista, FM ;
Campelo, JM ;
Garcia, A ;
Luna, D ;
Marinas, JM ;
Romero, AA ;
Urbano, MR .
JOURNAL OF CATALYSIS, 1997, 172 (01) :103-109
[4]   N-alkylation of aniline with methanol over AlPO4-Al2O3 catalysts [J].
Bautista, FM ;
Campelo, JM ;
Garcia, A ;
Luna, D ;
Marinas, JM ;
Romero, AA .
APPLIED CATALYSIS A-GENERAL, 1998, 166 (01) :39-45
[5]  
Bautista FM, 1997, STUD SURF SCI CATAL, V108, P123
[6]   Theoretical study of the mechanism of surface methoxy and dimethyl ether formation from methanol catalyzed by zeolitic protons [J].
Blaszkowski, SR ;
vanSanten, RA .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (13) :2292-2305
[7]  
Bosácek V, 1999, MAGN RESON CHEM, V37, pS135, DOI 10.1002/(SICI)1097-458X(199912)37:13<S135::AID-MRC562>3.0.CO
[8]  
2-Y
[9]   Surface NMR using laser-polarized 129Xe under magic angle spinning conditions [J].
Brunner, E ;
Seydoux, R ;
Haake, M ;
Pines, A ;
Reimer, JA .
JOURNAL OF MAGNETIC RESONANCE, 1998, 130 (01) :145-148
[10]   Study of the conversion of methanol to dimethyl ether on zeolite HZSM-5 using in situ flow MAS NMR [J].
Carlson, LK ;
Isbester, PK ;
Munson, EJ .
SOLID STATE NUCLEAR MAGNETIC RESONANCE, 2000, 16 (1-2) :93-102