Tppms

Using the OPENCORE NMR spectrometer, standard solid-state NMR experiments have been demonstrated in Ref. 2. They include 1H-13C CPMAS with TPPM decoupling, 13C-15N dipolar recoupling under MAS, 1H FSLG, 13C-13C 2D exchange, and so on. Here we show two more examples, where the spectrometer was used to implement standard pulse sequences, but in somewhat demanding circumstances in terms of sensitivity. 

The spectrometer supports phase cycling, asynchronous sequence implementation, and parameter-array experiments. Thus, most standard solid-state NMR experiments are feasible, including CPMAS, multiple-pulse H decoupling such as TPPM, 2D experiments, multiple-quantum NMR, and so on. In addition, the focus of development is on its extension of, or modification to, the hardware and/or the software, in the spirit of enabling the users to put their own new ideas into practice. In this paper, several examples of such have been described. They include the compact NMR and MRI systems, active compensation of RF pulse transients, implementation of a network analyzer, dynamic receiver-gain increment,31 and so on. 

Fig. 5 Radio frequency pulse sequences for measurements of Sj and Si in DSQ-REDOR experiments. The MAS period rR is 100 ps. XY represents a train of 15N n pulses with XY-16 phase patterns [98]. TPPM represents two-pulse phase modulation [99]. In these experiments, M = Nt 4, N2+ N3 = 48, and N2 is incremented from 0 to 48 to produce effective dephasing times from 0 to 9.6 ms. Signals arising from intraresidue 15N-13C DSQ coherence (Si) are selected by standard phase cycling. Signal decay due to the pulse imperfection of 15N pulses is estimated by S2. Decay due to the intermolecular 15N-I3C dipole-dipole couplings is calculated as Si(N2)/S2(N2). The phase cycling scheme can be found in the original figure and caption. (Figure and caption adapted from [45])...

Extraction of Active Catalyst Using TPPMS and Conditioning Agent. 

The water-soluble analogue of Wilkinson s catalyst, [RhCl(TPPMS)3] [TPPMS = PPh2(C6H4S03Na)], prepared in situ from Rh(/<-Cl)(diene)]2 and TPPMS, reacts with hydrogen in aqueous solution to yield [RhH(TPPMS)3], instead of [RhH2(TPPMS)3], according to Eq. (6) ... 

The presence of [RhH(TPPMS)3] causes substantial changes in the mechanism of hydrogenation, that most probably follows a conventional monohydride mechanism as shown in Scheme 1.1. This is also reflected in the rates and the hydrogenation selectivities [27]. 

Much emphasis has been placed in recent times on easily recoverable liquid bi-phasic catalysts, including metal clusters in nonconventional solvents. For instance, aqueous solutions of the complexes [Ru3(CO)12.x(TPPTS)x] (x=l, 2, 3 TPPTS = triphenylphosphine-trisulfonate, P(m-C6H4S03Na)3) catalyze the hydrogenation of simple alkenes (1-octene, cyclohexene, styrene) at 60°C and 60 bar H2 at TOF up to 500 h 1 [24], while [Ru i(CO)C (TPPMS) >,] (TPPMS = triphenylphos-phine-monosulfonate, PPh2(m-C6H4S03Na) is an efficient catalyst precursor for the aqueous hydrogenation of the C=C bond of acrylic acid (TOF 780 h 1 at 40 °C and 3 bar H2) and other activated alkenes [25]. The same catalysts proved to be poorly active in room temperature ionic liquids such as [bmim][BF4] (bmim= Tbutyl-3-methylimidazolium). No details about the active species involved are known at this point. 

The use of water-soluble ligands was referred to previously for both ruthenium and rhodium complexes. As in the case of ruthenium complexes, the use of an aqueous biphasic system leads to a clear enhancement of selectivity towards the unsaturated alcohol [34]. Among the series of systems tested, the most convenient catalysts were obtained from mixtures of OsCl3 3H20 with TPPMS (or better still TPPTS) as they are easily prepared and provide reasonable activities and modest selectivities. As with their ruthenium and rhodium analogues, the main advantage is the ease of catalyst recycling with no loss of activity or selectivity. However, the ruthenium-based catalysts are far superior. 

The use of water-soluble metal catalysts for the hydrogenation of thiophenes in aqueous biphasic systems has been primarily introduced by Sanchez-Delgado and coworkers at INTEVEP S.A. [61]. The precursors RuHC1(TPPTS)2(L2) (TPPTS=triphenylphosphine trisulfonate L=aniline, 1,2,3,4-tetrahydroquinoline) and RuHC1(TPPMS)2(L2) (TPPMS=triphenylphosphine monosulfonate) were... 

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