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21
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33846496589
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tBu derivatives) have been prepared in a similar manner and shown to have dimeric structures with elongated E-E bonds: Chivers, T.; Eisler, D. J.; Ritch, J. S. Manuscript in preparation.
-
tBu derivatives) have been prepared in a similar manner and shown to have dimeric structures with elongated E-E bonds: Chivers, T.; Eisler, D. J.; Ritch, J. S. Manuscript in preparation.
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33846522733
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All basis sets were used as they are referenced in the Turbomole 5.8 internal basis set library. Ahlrichs, R, et al. TURBOMOLE, Program Package for ab initio Electronic Structure Calculations, Version 5.8; Theoretical Chemistry Group, University of Karlsruhe: Karlsruhe, Germany, 2005
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All basis sets were used as they are referenced in the Turbomole 5.8 internal basis set library. Ahlrichs, R.; et al. TURBOMOLE, Program Package for ab initio Electronic Structure Calculations, Version 5.8; Theoretical Chemistry Group, University of Karlsruhe: Karlsruhe, Germany, 2005.
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33
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0001241599
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This type of bonding interaction is well established in the solid-state structures of halide salts of certain cationic sulfur-nitrogen ring systems, e.g, 1,2,3,4-dithiadiazolylium chlorides [RCN2S2]Cl and [S4N3]Cl: (a) Rawson, J. R, Banister, A. J, Lavender, I. Adv. Heterocycl. Chem. 1995, 62, 137
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42
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33846539569
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31 Te-Te 2.74, Te-I 2.70, Te-Cl 2.36, Te-F 1.95, Se-Se 2.34, Se-I 2.50, Se-F 1.77.
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31 Te-Te 2.74, Te-I 2.70, Te-Cl 2.36, Te-F 1.95, Se-Se 2.34, Se-I 2.50, Se-F 1.77.
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44
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33846558351
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36
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36
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48
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0001171082
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33846479170
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Cea-Olivares, R.1
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50
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33846516209
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39 but details of the crystallographic and structural data have not been reported.
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39 but details of the crystallographic and structural data have not been reported.
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53
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0037121888
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and references therein
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Briand, G. G.; Chivers, T.; Krahn, M.; Parvez, M. Inorg. Chem. 2002, 41, 6808 and references therein.
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Briand, G.G.1
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54
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33846489452
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43
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43
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55
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33846540041
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31P NMR spectrum), thus precluding the unlikely possibility that THF is the source of oxygen in the formation of 12.
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31P NMR spectrum), thus precluding the unlikely possibility that THF is the source of oxygen in the formation of 12.
-
-
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56
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33846552191
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The syntheses of the following related acyclic compounds EP(R 2)NP(R2)X (E, chalcogen; X, halogen) have been reported without structural characterization: [SP(Ph2)N(Ph2)PCl, 45a [SP(Ph2)N(Ph2)PCl]HCl,45a [SP(Ph2)N(Ph2)PBr],45b [OP(Ph 2)N(Ph2)PCl],45c and [OP(Ph2) N(Ph2)PBr]Br.45d
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45d
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