R12_2^5-2d: 2D DQ/SQ correlation R12₂⁵ pulse program for TopSpin2.1

Since non-phase cycling is applied to the R12₂⁵ excitation pulse, four-phase cycling is applied to the detection pulse P1 for selecting the 0Q -> -1Q coherence order jump, and four-phase cycling is applied to the R12₂⁵ reconversion pulse for filtering DQ coherences.

;r12-2-5_2d (TopSpin 2.0)

;2D SQ-DQ correlation experiment with R12_2^5, use r12-2-5_1d for setup
;M. Carravetta, M. Eden, X. Zhao, A. Brinkmann and M.H. Levitt, 
;Symmetry principles for the design of radiofrequency pulse seqeunces in
;the nuclear magnetic resonance of rotating solids, Chem. Phys. Lett 321 (2000) 205-215 
;by JOS 02/28/03

;Avance II+ version
;parameters:
;d1  : recycle delay
;d0  : incremented delay (2D) [1 usec]
;d20 : delay between saturation pulses

;p1 : detection pulse with pl1 power

;pl1  : f1 power level
;pl11 : for R12_2^5 recoupling sequence B1=(N/2n)*cnst31=3*cnst31 in Hz

;cnst31 : spinning speed
;l0  : number of basic R12_2^5 cycles for DQ excitation
;l3  : number of rotor period for DQ evolution
;l20 : # of pulses in saturation pulse train
;in0 : l3*rotorperiod=l3*(1/cnst31), t1 increment
;ns  : n*16
;FnMode : undefined
;mc2 : STATES-TPPI
;nd0 : 1
;zgoptns :-Dpresat or blank

;$COMMENT=SQ-DQ experiment with R12_2^5
;$CLASS=Solids
;$DIM=2D
;$TYPE=direct excitation
;$SUBTYPE=homonuclear correlation
;$OWNER=Bruker

define loopcounter count    ;for STATES-TPPI procedure
  "count=td1/2"             ;and STATES cos/sin procedure
                            
define pulse pul180
  "pul180=(1.0s/cnst31)/6"  ;180° pulse

  "d31=1s/cnst31"
  "d0=1u"
  "in0=l3*d31"
  "inf1=l3*d31"

;cnst11 : to adjust t=0 for acquisition, if digmod = baseopt
"acqt0=1u*cnst11"

#include <rot_prot.incl>

  ze                        ;acquire into a cleared memory
1 d31

#ifdef presat               ;set with -Dpresat
pres, d20                   ;delay between saturation pulses
  (p1 pl1 ph1):f1           ;saturation loop if required
  lo to pres times l20
#endif /* presat */

2 d1                        ;recycle delay
  1m rpp11                  ;reset the phase ph11 pointer to the first element
                            ;in the DQ excitation pulse
  1m rpp13                  ;reset the phase ph13 pointer to the first element
                            ;in the DQ reconversion pulse
  10u reset:f1
  1u pl11:f1                ;switch to R12_2^5 RF condition

                            ;R12_2^5 DQ excitation
3 (pul180  ph11 ipp11):f1   ;increment phase ph11 pointer
  (pul180  ph11 ipp11):f1   ;increment phase ph11 pointer
  lo to 3 times l0

  d0                        ;DQ evolution

                            ;R12_2^5 DQ reconversion
4 (pul180  ph13 ipp13):f1   ;increment phase ph13 pointer
  (pul180  ph13 ipp13):f1   ;increment phase ph13 pointer
  lo to 4 times l0

  (p1 pl1 ph5):f1           ;detection pulse
  gosc ph31                 ;gosc does not loop to 1

                            ;DQ filtering (four phase cycling):
  1m ip13*16384             ;increments all phases of ph13 by 90°

  lo to 1 times ns          ;next scan
  100m wr #0 if #0 zd       ;save data

  1m ip11*8192              ;increments all phases of ph11 by 45°, 
                            ;90° phase for DQ coherence
  lo to 1 times 2           ;t1 quadrature detection

  1m id0                    ;increment in l3*rotorperiod

  ;1m rp11                  ;reset all phases of ph11 and ph13 
                            ;to their original values, i.e. to the values they 
  ;1m rp13                  ;had before the first ip11 and ip13
                            ;in case of STATES remove semicolon at beginning of the 2 lines

  lo to 1 times count       ;count=td1/2
HaltAcqu, 1m
exit

ph1=0                       ;for saturation pulse

ph11=(65536) 13653  51883   ; 75°  285°  or  75°   -75°
ph13=(65536) 30037   2731   ;165°   15°  or  ph11 + 90°

ph5= 0 0 0 0 2 2 2 2 1 1 1 1 3 3 3 3
ph31=0 2 0 2 2 0 2 0 1 3 1 3 3 1 3 1
  

Example1: ³¹P in VPI-5 zeolite with AV500

³¹P MAS FID of VPI-5 zeolite. Its duration is about 4 msec.

³¹P MAS spectra of VPI-5 zeolite versus the excitation pulse p1 duration (pl1 = 9.5 dB) in zg pulse program, acquired with a 4-mm diameter rotor spinning at 15 kHz, D1 = 10 sec recycle delay, and recorded with Bruker Avance III, 500 MHz WB US magnet.

Pulseprogram parameters for zg:

³¹P MAS spectra of VPI-5 zeolite versus the excitation pulse p1 duration (pl1 = 9.5 dB) in zgsat.gul pulse program, acquired with a 4-mm diameter rotor spinning at 15 kHz, and recorded with Bruker Avance III, 500 MHz.

Pulseprogram parameters for zgsat.gul:

³¹P MAS spectra of VPI-5 zeolite versus the excitation power pl11 (l0 = 50) in r12-2-5_1d.ppm, acquired with a 4-mm diameter rotor spinning at 15 kHz, and recorded with Bruker Avance III, 500 MHz.

Pulseprogram parameters for r12-2-5_1d.ppm:

³¹P MAS spectra of VPI-5 zeolite versus the number l0 of basic unit (pl11 = 11.4 dB) in r12-2-5_1d.ppm, acquired with a 4-mm diameter rotor spinning at 15 kHz, and recorded with Bruker Avance III, 500 MHz.

Pulseprogram parameters for r12-2-5_1d.ppm:

³¹P R12_2^5 DQ/SQ spectrum of VPI-5 zeolite acquired with a 4-mm diameter rotor spinning at 15 kHz, ino = 1/cnst31, and recorded with Bruker Avance III, 500 MHz. MC2 = STATES-TPPI.

Pulseprogram parameters for r12-2-5_2d.ppm:

Acquisition parameters:

³¹P R12_2^5 DQ/SQ spectrum of VPI-5 zeolite acquired with a 4-mm diameter rotor spinning at 15 kHz, ino = 2*pul180, and recorded with Bruker Avance III, 500 MHz. MC2 = STATES.

³¹P R12_2^5 DQ/SQ spectrum of VPI-5 zeolite acquired with a 4-mm diameter rotor spinning at 15 kHz, ino = 2*pul180, and recorded with Bruker Avance III, 500 MHz. MC2 = STATES-TPPI.

Pulseprogram parameters for r12-2-5_2d.ppm:

Acquisition parameters:

³¹P R12_2^5 DQ/SQ spectrum of VPI-5 zeolite acquired with a 4-mm diameter rotor spinning at 15 kHz, inf1 = p9 = 1/cnst31, and recorded with Bruker Avance III, 500 MHz. MC2 = STATES-TPPI.

Pulseprogram parameters for r12-2-5_2dbsw.ppm:

Acquisition parameters:

³¹P R12_2^5 DQ/SQ spectrum of VPI-5 zeolite acquired with a 4-mm diameter rotor spinning at 15 kHz, inf1 = p9 = 2*pul180, and recorded with Bruker Avance III, 500 MHz. MC2 = STATES-TPPI.

Pulseprogram parameters for r12-2-5_2dbsw.ppm:

Acquisition parameters:

Example2: ¹H in L-tyrosine with AV700

¹H MAS spectra of adamantane versus the excitation pulse p1 duration (pl1 = 4 dB), recycle delay D1 = 10 s, acquired with a 1.3-mm diameter rotor spinning at 60 kHz, and recorded with Bruker Avance III, 700 MHz. Adamantane proton full spectrum.

Pulseprogram parameters for zg:

¹H MAS FID of L-tyrosine acquired with a 1.3-mm diameter rotor spinning at 60 kHz, and recorded with Bruker Avance III, 700 MHz.

¹H MAS spectrum of L-tyrosine acquired with a 1.3-mm diameter rotor spinning at 60 kHz, and recorded with Bruker Avance III, 700 MHz.

Pulseprogram parameters for zg:

¹H MAS spectra of L-tyrosine versus the number l0 of basic unit (pl11 = 4.6 dB) in r12-2-5_1d.ppm, acquired with a 1.3-mm diameter rotor spinning at 60 kHz, and recorded with Bruker Avance III, 700 MHz.

Pulseprogram parameters for r12-2-5_1d.ppm:

¹H MAS spectra of L-tyrosine versus the excitation power pl11 (l0 = 7) in r12-2-5_1d.ppm, acquired with a 1.3-mm diameter rotor spinning at 60 kHz, and recorded with Bruker Avance III, 700 MHz.

Pulseprogram parameters for r12-2-5_1d.ppm:

¹H R12_2^5 DQ/SQ ser file of L-tyrosine acquired with a 1.3-mm diameter rotor spinning at 60 kHz, ino = 2/cnst31, and recorded with Bruker Avance III, 700 MHz.

¹H R12_2^5 DQ/SQ spectrum of L-tyrosine acquired with a 1.3-mm diameter rotor spinning at 60 kHz, ino = 2/cnst31, and recorded with Bruker Avance III, 700 MHz. MC2 = STATES-TPPI.

Pulseprogram parameters for r12-2-5_2d.ppm:

Acquisition parameters:

References

1. Lena Seyfarth and Jürgen Senker
   An NMR crystallographic approach for the determination of the hydrogen substructure of nitrogen bonded protons,
   Phys. Chem. Chem. Phys. 11, 3522-3531 (2009).
   Abstract
2. M. Carravetta, A. Danquigny, S. Mamone, F. Cuda, O. G. Johannessen, I. Heinmaa, K. Panesar, R. Stern, M. C. Grossel, A. J. Horsewill, A. Samoson, M. Murata, Y. Murata, K. Komatsu, and M. H. Levitt
   Solid-state NMR of endohedral hydrogen-fullerene complexes,
   Phys. Chem. Chem. Phys. 9, 4879-4894 (2007).
   Abstract
3. M. Carravetta, M. Edén, O. G. Johannessen, H. Luthman, P. J. E. Verdegem, J. Lugtenburg, A. Sebald, and M. H. Levitt
   Estimation of carbon-carbon bond lengths and medium-range internuclear distances by solid-state nuclear magnetic resonance,
   J. Am. Chem. Soc. 123, 10628-10638 (2001).
   Abstract
4. Marina Carravetta, Mattias Edén, Xin Zhao, Andreas Brinkmann, and Malcolm H. Levitt
   Symmetry principles for the design of radiofrequency pulse sequences in the nuclear magnetic resonance of rotating solids,
   Chem. Phys. Lett. 321, 205-215 (2000).
   Abstract

Other references

1. Subhradip Paul, Rajendra Singh Thakur, M. H. Levitt, and P. K. Madhu
   ¹H homonuclear dipolar decoupling using rotor-synchronised pulse sequences: Towards pure absorption phase spectra, (RN_n^N/2)
   J. Magn. Reson. 205, 269-275 (2010).
   Abstract
2. Mattias Edén
   Two-dimensional MAS NMR correlation protocols involving double-quantum filtering of quadrupolar spin-pairs, (R2₂¹; R2₄¹)
   J. Magn. Reson. 204, 99-110 (2010).
   Abstract
3. B. Hu, L. Delevoye, O. Lafon, J. Trébosc, and J. P. Amoureux
   Double-quantum NMR spectroscopy of ³¹P species submitted to very large CSAs, (BR2₂¹; BABA-4; SPIP; fp-RFDR)
   J. Magn. Reson. 200, 178-188 (2009).
   Abstract
4. Q. Wang, B. Hu, O. Lafon, J. Trébosc, F. Deng, and J. P. Amoureux
   Double-quantum homonuclear NMR correlation spectroscopy of quadrupolar nuclei subjected to magic-angle spinning and high magnetic field, (BR2₂¹; SR2₂¹)
   J. Magn. Reson. 200, 251-260 (2009).
   Abstract
5. Mattias Edén and Andy Y. H. Lo
   Supercycled symmetry-based double-quantum dipolar recoupling of quadrupolar spins in MAS NMR: I. Theory, (R2₂¹; R2₄¹; R4₄²; C1₂⁰; C2₄¹)
   J. Magn. Reson. 200, 267-279 (2009).
   Abstract
6. Jakob J. Lopez, Christoph Kaiser, Sarika Shastri, and Clemens Glaubitz
   Double quantum filtering homonuclear MAS NMR correlation spectra: a tool for membrane protein studies, (R22₄⁹)
   J. Biomol. 41, 97-104 (2008).
   Abstract
7. Gregor Mali, Venčeslav Kaučič, and Francis Taulelle
   Measuring distances between half-integer quadrupolar nuclei and detecting relative orientations of quadrupolar and dipolar tensors by double-quantum homonuclear dipolar recoupling nuclear magnetic resonance experiments, (R2₂¹)
   J. Chem. Phys. 128, 204503/1-204503/11 (2008).
   Abstract
8. Darren H. Brouwer, Per Eugen Kristiansen, Colin A. Fyfe, and Malcolm H. Levitt
   Symmetry-based ²⁹Si dipolar recoupling magic angle spinning NMR spectroscopy: A new method for investigating three-dimensional structures of zeolite frameworks, (SR26₄¹¹)
   J. Am. Chem. Soc. 127, 542-543 (2005).
   Abstract
9. Mattias Edén, Hans Annersten, and Åsa Zazzi
   Pulse-assisted homonuclear dipolar recoupling of half-integer quadrupolar spins in magic-angle spinning NMR, (R4₄¹)
   Chem. Phys. Lett. 410, 24-30 (2005).
   Abstract
10. Per Eugen Kristiansen, Marina Carravetta, Wai Cheu Lai, and Malcolm H. Levitt
    A robust pulse sequence for the determination of small homonuclear dipolar couplings in magic-angle spinning NMR, (SR26₄¹¹)
    Chem. Phys. Lett. 390, 1-7 (2004).
    Abstract
11. Per Eugen Kristiansen, Dan J. Mitchell, and Jeremy N. S. Evans
    Double-quantum dipolar recoupling at high magic-angle spinning rates, (RN)
    J. Magn. Reson. 157, 253-266 (2002).
    Abstract
12. Andreas Brinkmann, Jörn Schmedt auf der Günne, and Malcolm H. Levitt
    Homonuclear zero-quantum recoupling in fast magic-angle spinning nuclear magnetic resonance, (R6₆²)
    J. Magn. Reson. 156, 79-96 (2002).
    Abstract

Solid-state NMR bibliography for: