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Improved methods for three-dimensional TROSY-Type HCCH correlation involving protons of negligible CSA are presented. The TROSY approach differs from the conventional approach of heteronuclear decoupling in evolution and detection periods by not mixing fast and slowly relaxing coherences and usually suppressing the former. Pervushin et al. (J. Am. Chem. Soc. 120, 6394–6400 (1998)) have proposed a 3D TROSY-type HCCH experiment where the TROSY approach is applied only in one of the 13C dimensions. A new pulse sequence applying the TROSY approach in both indirect dimensions is advantageous when the TROSY effect of the carbons is large or when a relatively high resolution is required. For lower resolutions or moderate TROSY effects we show that it is possible to combine the best of both worlds, namely to suppress heteronuclear couplings without mixing fast and slowly relaxing coherences while at the same time superimpose the two components and thus have both contribute to the detected signal. That is possible using the novel technique of Spin-State-Selective Time-Proportional Phase Incrementation (S3 TPPI). The new 3D S3 TPPI TROSY HCCH method is demonstrated on a 13C,15N-labeled protein sample, RAP 18–112 (N-terminal domain of α2-macroglobulin receptor associated protein), at 750 MHz and average sensitivity enhancements of 10% are obtained for the cross peaks in comparison to methods based on conventional decoupling on one of the carbons or on TROSY on both carbons.  相似文献   
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The normal isotopomer and three additional isotopic species of the OCS–(HCCH)2 trimer have been observed by pulsed nozzle Fourier transform microwave spectroscopy. Semi-empirical modeling predicts a structure that has the two acetylene monomers aligned in a geometry between the well-known T-shaped orientation of the acetylene dimer and a parallel intermediate. Rotational constants and dipole moment measurements are consistent with this model.  相似文献   
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