The influence of the molecular system on the performance of heteronuclear decoupling in solid-state NMR

被引:6
|
作者
Gerbaud, Guillaume [1 ]
Caldarelli, Stefano [1 ]
Ziarelli, Fabio [2 ]
Gastaldi, Stephane [3 ]
机构
[1] Aix Marseille Univ, UMR 6263, ISm2, F-13013 Marseille, France
[2] Univ Aix Marseille 3, F-13628 Aix En Provence, France
[3] Univ Paul Cezanne, Fac Sci St Jerome, LCP UMR 6264, Equipe Chim Mol Organ, F-13397 Marseille 20, France
关键词
Solid-state NMR; Heteronuclear decoupling; CPMAS; TPPM; GTn; NUCLEAR-MAGNETIC-RESONANCE; LIQUID-CRYSTALS; LINEWIDTHS; FREQUENCY; SEQUENCES;
D O I
10.1016/j.jmr.2011.02.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The intensity of the carbon signal in a CPMAS experiment has been measured for two CH and three CH2 moieties in four test molecules under different phase-modulated proton decoupling conditions and as a function of the spinning rate. The proton decoupling schemes investigated were the golden standard TPPM and three of the GTn family. Aim of this analysis was to better describe experimentally the impact and limitations of phase-modulated decoupling. Sizeable differences in the response to decoupling were observed in otherwise chemically identical molecular fragments, such as the CHCH2 found in tyrosine, phenyl-succinic acid or 9-Anthrylmethyl-malonate, probably due to differences in spin-diffusion rates. In keeping with known facts, the efficiency of the decoupling was observed to decrease with the MAS rate, but with somewhat different trends for the tested systems. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:75 / 81
页数:7
相关论文
共 50 条
  • [1] On the choice of heteronuclear dipolar decoupling scheme in solid-state NMR
    Paul, Subhradip
    Kurur, N. D.
    Madhu, P. K.
    JOURNAL OF MAGNETIC RESONANCE, 2010, 207 (01) : 140 - 148
  • [2] Efficiency of heteronuclear dipolar decoupling schemes in solid-state NMR: Investigation of effective transverse relaxation times
    Mithu, Venus Singh
    Pratihar, Supriya
    Paul, Subhradip
    Madhu, P. K.
    JOURNAL OF MAGNETIC RESONANCE, 2012, 220 : 8 - 17
  • [3] Rationalising Heteronuclear Decoupling in Refocussing Applications of Solid-State NMR Spectroscopy
    Frantsuzov, Ilya
    Vasa, Suresh K.
    Ernst, Matthias
    Brown, Steven P.
    Zorin, Vadim
    Kentgens, Arno P. M.
    Hodgkinson, Paul
    CHEMPHYSCHEM, 2017, 18 (04) : 394 - 405
  • [4] Efficient heteronuclear decoupling in MAS solid-state NMR using non-rotor-synchronized rCW irradiation
    Equbal, Asif
    Paul, Subhradip
    Mithu, Venus Singh
    Madhu, P. K.
    Nielsen, Niels Chr.
    JOURNAL OF MAGNETIC RESONANCE, 2014, 246 : 104 - 109
  • [5] A unified heteronuclear decoupling strategy for magic-angle-spinning solid-state NMR spectroscopy
    Equbal, Asif
    Bjerring, Morten
    Madhu, P. K.
    Nielsen, Niels Chr.
    JOURNAL OF CHEMICAL PHYSICS, 2015, 142 (18)
  • [6] Frequency-swept pulse sequences for 19F heteronuclear spin decoupling in solid-state NMR
    Chandran, C. Vinod
    Madhu, P. K.
    Wormald, Philip
    Braeuniger, Thomas
    JOURNAL OF MAGNETIC RESONANCE, 2010, 206 (02) : 255 - 263
  • [7] Heteronuclear Spin Decoupling in Solid-State Nuclear Magnetic Resonance: Overview and Outlook
    Madhu, P. K.
    ISRAEL JOURNAL OF CHEMISTRY, 2014, 54 (1-2) : 25 - 38
  • [8] Refocusing pulses: A strategy to improve efficiency of phase-modulated heteronuclear decoupling schemes in MAS solid-state NMR
    Jain, Mukul G.
    Sreedevi, K. N.
    Equbal, Asif
    Madhu, P. K.
    Agarwal, Vipin
    JOURNAL OF MAGNETIC RESONANCE, 2017, 284 : 59 - 65
  • [9] Efficient heteronuclear dipolar decoupling in solid-state NMR using frequency-swept SPINAL sequences
    Chandran, C. Vinod
    Braeuniger, Thomas
    JOURNAL OF MAGNETIC RESONANCE, 2009, 200 (02) : 226 - 232
  • [10] Refocused continuous-wave decoupling: A new approach to heteronuclear dipolar decoupling in solid-state NMR spectroscopy
    Vinther, Joachim M.
    Nielsen, Anders B.
    Bjerring, Morten
    van Eck, Ernst R. H.
    Kentgens, Arno P. M.
    Khaneja, Navin
    Nielsen, Niels Chr.
    JOURNAL OF CHEMICAL PHYSICS, 2012, 137 (21)