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It is unknown whether or not there exists an [87, 5, 57; 3]-code. Such a code would meet the Griesmer bound. The purpose of this paper is to give a constructive proof of the existence of [q
4 + q
2 – q, 5, q
4 – q
3 + q
2 – 2q; q]-codes for any prime power q 3. As a special case, it is shown that there exists an [87, 5, 57; 3]-code with weight enumerator 1 + 156z
37 + 82z
60 + 2z
63 + 2z
78. The new construction settles an open problem due to Hill and Newton [10]. 相似文献
87.
Yosi Kratish Dr. Arseni Kostenko Alexander Kaushansky Dr. Boris Tumanskii Dr. Dmitry Bravo‐Zhivotovskii Prof. Dr. Yitzhak Apeloig 《Angewandte Chemie (International ed. in English)》2018,57(27):8275-8279
The first persistent platinum(I)‐centered radical was generated by homolytic cleavage of a Pt?HgSiR3 bond of a mercury‐substituted platinum(II) complex. The PtI radical was characterized by EPR spectroscopy, chemical trapping experiments, and density functional theory (DFT) calculations. 相似文献
88.
Journal of Algebraic Combinatorics - Let p be a prime number. Reducible cyclic codes of rank 2 over $$\mathbb {Z}_{p^m}$$ are shown to have exactly two Hamming weights in some cases. Their weight... 相似文献
89.
The two major fundamental obstacles which so far have prevented theisolation of stable silynes, RSiCR (1), are: (a)the existence of more stable isomers, e.g., RRC=Si: (2) and(b) their extremely facile (exothermic) dimerication. The steric andelectronic effects of various substituents R and R (R = alkoxy,alkyl, aryl and silyl; R = alkyl and aryl groups) on the stability ofRSiCR relative to the isomeric RRC=Si:(E(1-2)), and on the energy of dimerization tothe corresponding 1,3-disilacyclobutadienes (E(D)), werestudied computationally using density functional theory (DFT) and theONIOM method. The goal was to find a combination of substituents thatwill make RSiCR more stable than RRC=Si: and whichwill also prevent its dimerization. For R = R = H,E(1-2)) = 40.7 kcal/mol (i.e., 2 islower in energy than 1), and E(D) = –104.0kcal/mol. 1, R = OH, R = m-Tbt 2,6-bis[bis(silyl)methyl]phenyl, is by 11.1 kcal/mol morestable than the isomeric silylidene 2. However, thedimerization of 1, R = OH, R = m-Tbt remains highlyexothermic (by 101 kcal/mol). 1, R = R = m-Tbt and1, R = (t-Bu)3Si, R = m-Tbt, are by 5.8 and 2.0kcal/mol, respectively, less stable than the corresponding 2.However, the dimerization of 1, R = (t-Bu)3Si, = m-Tbt is exothermic by only 12 kcal/mol. For1, R = (t-Bu)3Si, and R = Tbt 2,6-bis[bis(trimethylsilyl)methyl]phenyl, the corresponding1,3-disilacyclobutadiene dimer 3, dissociates spontaneously.Thus, (t-Bu3Si)SiCTbt is predicted to be kineticallystable towards both, isomerization to (t-Bu3Si)TbtC=Si: anddimerization to 3, making it a viable synthetic target. Thereported energies were calculated atB3LYP/6-31G**//B3LYP/3-21G*; good agreement is found betweenthe DFT and the ONIOM results. 相似文献
90.
Twelve 11C-labelled amines were prepared via 11C-carbonylation followed by reductive amination. The 11C-carbonylation was performed in the presence of tetrakis(triphenylphosphine)palladium using aryl iodides or aryl triflates, [11C]carbon monoxide and phenyl-/methylboronic acid. The [11C]ketones formed in this step were then transformed directly into amines by reductive amination using different amines in the presence of TiCl4 and NaBH3CN. The 11C-labelled amines were obtained with decay-corrected radiochemical yields in the range 2-78%. The radiochemical purity of the isolated products exceeded 98%. (13C)Benzhydryl-phenyl-amine was synthesised and analysed by NMR spectroscopy for confirmation of the labelling position. Specific radioactivity was determined for the same compound. The reference compounds were prepared by reductive amination of ketones using conventional reaction conditions and three of the compounds were novel. The presented approach is a new method for the synthesis of [11C]/(13C)amines. 相似文献