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Volumn 45, Issue 26, 2006, Pages 10678-10687

Synthesis, spectroscopic, and structural investigation of the cyclic [N(PR2E)2]+ cations (E = Se, Te; R = iPr, Ph): The effect of anion and R-group exchange

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EID: 33846483753     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic061545i     Document Type: Article
Times cited : (26)

References (60)
  • 4
    • 0034799750 scopus 로고    scopus 로고
    • For reviews of early work, see a
    • For reviews of early work, see (a) Silvestru, C.; Drake, J. E. Coord. Chem. Rev. 2001, 223, 117.
    • (2001) Coord. Chem. Rev , vol.223 , pp. 117
    • Silvestru, C.1    Drake, J.E.2
  • 6
    • 11144330615 scopus 로고    scopus 로고
    • McCleverty, J. A, Meyer, T. J, Eds, Elsevier Ltd: Amsterdam
    • (c) Haiduc, I. In Comprehensive Coordination Chemistry II; McCleverty, J. A., Meyer, T. J., Eds.; Elsevier Ltd: Amsterdam, 2003; pp 323-347.
    • (2003) Comprehensive Coordination Chemistry II , pp. 323-347
    • Haiduc, I.1
  • 21
    • 33846496589 scopus 로고    scopus 로고
    • 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.
  • 31
    • 33846522733 scopus 로고    scopus 로고
    • 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
    • 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.
  • 32
    • 33846493984 scopus 로고    scopus 로고
    • Frisch, M. J, Trucks, G. W, Schlegel, H. B, Scuseria, G. E, Robb, M. A, Cheeseman, J. R, Montgomery, J. A, Jr, Vreven, T, Kudin, K. N, Burant, J. C, Millam, J. M, Iyengar, S. S, Tomasi, J, Barone, V, Mennucci, B, Cossi, M, Scalmani, G, Rega, N, Petersson, G. A, Nakatsuji, H, Hada, M, Ehara, M, Toyota, K, Fukuda, R, Hasegawa, J, Ishida, M, Nakajima, T, Honda, Y, Kitao, O, Nakai, H, Klene, M, Li, X, Knox, J. E, Hratchian, H. P, Cross, J. B, Bakken, V, Adamo, C, Jaramillo, J, Gomperts, R, Stratmann, R. E, Yazyev, O, Austin, A. J, Cammi, R, Pomelli, C, Ochterski, J. W, Ayala, P. Y, Morokuma, K, Voth, G. A, Salvador, P, Dannenberg, J. J, Zakrzewski, V. G, Dapprich, S, Daniels, A. D, Strain, M. C, Farkas, O, Malick, D. K, Rabuck, A. D, Raghavachari, K, Foresman, J. B, Ortiz, J. V, Cui, Q, Baboul, A. G, Clifford, S, Cioslowski, J, Stefanov, B. B, Liu, G, Liashenko, A, Piskorz, P, Komaromi, I, Martin, R. L, Fox, D. J, Keit
    • Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Montgomery, J. A., Jr.; Vreven, T.; Kudin, K. N.; Burant, J. C.; Millam, J. M.; Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi, M.; Scalmani, G.; Rega, N.; Petersson, G. A.; Nakatsuji, H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Klene, M.; Li, X.; Knox, J. E.; Hratchian, H. P.; Cross, J. B.; Bakken, V.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Ayala, P. Y.; Morokuma, K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M. C.; Farkas, O.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Ortiz, J. V.; Cui, Q.; Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Challacombe, M.; Gill, P. M. W.; Johnson, B.; Chen, W.; Wong, M. W.; Gonzalez, C.; Pople, J. A. Gaussian 03, revision C.02; Gaussian, Inc.: Wallingford, CT, 2004.
  • 33
    • 0001241599 scopus 로고    scopus 로고
    • 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
    • 3]Cl: (a) Rawson, J. R.; Banister, A. J.; Lavender, I. Adv. Heterocycl. Chem. 1995, 62, 137.
  • 37
    • 23244438347 scopus 로고    scopus 로고
    • 3: Klapötke, T. M.; Krumm, B.; Nöth, H.; Gálvez-Ruiz, J. C.; Polborn, K.; Schwab, I.; Suter, M. Inorg. Chem. 2005, 44, 5254.
    • 3: Klapötke, T. M.; Krumm, B.; Nöth, H.; Gálvez-Ruiz, J. C.; Polborn, K.; Schwab, I.; Suter, M. Inorg. Chem. 2005, 44, 5254.
  • 39
    • 33846495994 scopus 로고    scopus 로고
    • 29
    • 29
  • 42
    • 33846539569 scopus 로고    scopus 로고
    • 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.
    • 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.
  • 47
    • 33846558351 scopus 로고    scopus 로고
    • 36
    • 36
  • 50
    • 33846516209 scopus 로고    scopus 로고
    • 39 but details of the crystallographic and structural data have not been reported.
    • 39 but details of the crystallographic and structural data have not been reported.
  • 54
    • 33846489452 scopus 로고    scopus 로고
    • 43
    • 43
  • 55
    • 33846540041 scopus 로고    scopus 로고
    • 31P NMR spectrum), thus precluding the unlikely possibility that THF is the source of oxygen in the formation of 12.
    • 31P NMR spectrum), thus precluding the unlikely possibility that THF is the source of oxygen in the formation of 12.
  • 56
    • 33846552191 scopus 로고    scopus 로고
    • 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
    • 45d


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