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pro vyhledávání: '"T. Saluvere"'
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Publikováno v:
Field-Programmable Logic Architectures, Synthesis and Applications ISBN: 9783540584193
FPL
FPL
Spread spectrum digital radio receivers and transmitters are very difficult to simulate for overall system performance evaluation. Reliable estimates for Bit Error Rates and effect of indoor and outdoor fading radio channels can be best studied via p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9e77ec8c0bf24b7f4a6ac4afa8732d6
https://doi.org/10.1007/3-540-58419-6_83
https://doi.org/10.1007/3-540-58419-6_83
Publikováno v:
Advances in Molecular Relaxation Processes. 5:169-177
The 14N chemical shifts and NMR line widths are reported for some monosubstituted pyridines. The chemical shifts show a satisfactory correlation with the electronic nature of the substituents. By means of the average excitation energy approximation t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20868a15e203d5e74ccde70163acd338
https://doi.org/10.1016/0001-8716(73)80032-x
https://doi.org/10.1016/0001-8716(73)80032-x
Publikováno v:
Organic Magnetic Resonance. 5:429-436
Chemical polarisation of 13C and 15N nuclei in the thermal decomposition of diazoaminobenzene has been investigated. Most of the polarised products with the exception of benzene result from cage recombination processes, and both the 13C and 15N true
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5deee94b37ce1e973d01c8edfe91225
https://doi.org/10.1002/mrc.1270050909
https://doi.org/10.1002/mrc.1270050909
Autor:
B. D. Sviridov, V. V. Ershov, L. G. Plekhanova, Sh. A. Markaryan, Anatolii L Buchachenko, G. A. Nikiforov, Endel Lippmaa, T. Saluvere, Tõnis Pehk, S. V. Rykov
Publikováno v:
Organic Magnetic Resonance. 5:339-342
Thermal decomposition of 4-diazo-2,6-di-tert-butyl-2, 5-cyclohexadien-1-one in perhalogenated solvents has been investigated. The decomposition reaction proceeds via a carbene intermediate first to a singlet and then to an effectively triplet free en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a04d86a63f086fc76b0659412453d140
https://doi.org/10.1002/mrc.1270050707
https://doi.org/10.1002/mrc.1270050707
Publikováno v:
Molecular Physics. 23:1071-1081
The 14N chemical shifts of some monosubstituted pyridines are reported. They show a correlation with the electronic nature of the substituent which is not found with earlier 14N chemical shift data. The shifts may be satisfactorily explained in terms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::581fb8a9af261e14b6236e958ae264d2
https://doi.org/10.1080/00268977200101051
https://doi.org/10.1080/00268977200101051
Autor:
Endel Lippmaa, T. Saluvere
Publikováno v:
Chemical Physics Letters. 7:545-548
The spin-lattice relaxation of 15 N nuclei in inorganic ions is governed by inter- and intramolecular dipole-dipole and shift anisotropy interactions at lower temperatures and by the spin-rotation interaction at higher temperatures. The measured rela
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a81af863116ef2654ec79eaf90d6a6ff
https://doi.org/10.1016/0009-2614(70)80168-3
https://doi.org/10.1016/0009-2614(70)80168-3
Publikováno v:
Chemical Physics Letters. 11:120-123
The spin-lattice relaxation of 15 N nuclei in organic compounds is caused by the dipole-dipole interaction with protons at lower temperatures and by the spin-rotation interaction at higher temperatures. The relaxation times are very long in most comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::321ac57a968bb85a7963e18071366772
https://doi.org/10.1016/0009-2614(71)80547-x
https://doi.org/10.1016/0009-2614(71)80547-x
Publikováno v:
Magnetic Resonance and Related Phenomena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2198112c6a947bec653e213b7895e93
https://doi.org/10.1007/978-3-642-81344-3
https://doi.org/10.1007/978-3-642-81344-3