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- P. 2313-2327.457. Пат. US5708150, МПК C07F17/00; C07F17/02. Process for preparing transition metal complexes containing disubstituted cyclopentadienyl ligands [текст] / Lisowsky R. (Германия); заявитель WITCO GMBH; заявл. 22.12.1994 ; опубл. 13.01.1998. - 6 с. : илл.458. Пат. US2005148460, МПК C07F17/00; C08F10/00.
Catalyst components and their use in thepolymerization of olefins [текст] / Marin V., Razavi A. (США); заявитель Marin V., Razavi A.; заявл. 02.01.2004 ; опубл. 07.07.2005. - 21 с. : илл.459. Burger, P. ansa-Metallocene derivatives: XXIII . Aryl-substituted titanocene and zirconocenecomplexes with interannular tetramethylethano- or dimethylsilano-bridges. Crystal structures of representative examples [текст] / P. Burger, K.
Hortmann, J. Diebold, H.-H. Brintzinger // J. Organomet.Chem. - 1991. - V. 417. - № 1-2. - P. 9-27.460. Alder, K. Uber die Darstellung von Santen und anderen substituierten Bicyclo-[1.2.2]-heptenen[текст] / K. Alder, H.-J. Ache // Chem. Ber. - 1962. - B. 95. - № 2. - S. 503-510.461.
Clark, T. J. Synthesis and properties of sterically congested cyclopentadienes and their transitionmetal complexes [текст] / T. J. Clark, C. M. Killian, S. Luthra, T. A. Nile // J. Organomet. Chem. 1993. - V. 462. - № 1-2. - P. 247-257.462. Deno, N. C. Carbonium Ions. XIX. The Intense Conjugation in Cyclopropyl Carbonium Ions[текст] / N. C. Deno, H. G. Richey, J. S.
Liu, D. N. Lincoln, J. O. Turner // J. Am. Chem. Soc. 1965. - V. 87. - № 20. - P. 4533-4538.463. Gomez, F. J. Syndiospecific Propylene Polymerization Using C1-Symmetric ansa-MetalloceneCatalysts: Substituent and Bridge Effects [текст] / F. J. Gomez, R. M. Waymouth // Macromolecules.- 2002. - V. 35.
- № 9. - P. 3358-3368.464. Stone, K. J. An exceptionally simple and efficient method for the preparation of a wide variety offulvenes [текст] / K. J. Stone, R. D. Little // J. Org. Chem., 1984. - V. 49. - № 11. - P. 1849-1853.465. Drewitt, M. J. The first [2]cobaltocenophane and [2]metallocenophanium salts [текст] / M. J.Drewitt, S. Barlow, D. O'Hare, J. M. Nelson, P. N. I. Manners // Chem. Commun.
- 1996. - № 18. - P.2153-2154.403466. Moeller, A. C. Synthetic Explorations Towards Sterically Crowded 1,2,3-SubstitutedBis(indenyl)zirconium(IV) Dichlorides [текст] / A. C. Moeller, R. Blom, R. H. Heyn, O. Swang, C.H. Goerbitz, T. Seraidaris // Eur. J. Inorg. Chem. - 2005. - № 9. - P.
1759-1769.467. Cordes, J. F. Notiz uber eine einfache Methode zur Darstellung von Niccelocen und Cobaltocen[текст] / J. F. Cordes // Chem. Ber. - 1962. - B. 95. - № 12. - S. 3084-3085.468. Gmelin Handbook of Inorganic and Organometallic Chemistry [текст]: Ni (System-Nr. 57): Org.Verb. 2 - Springer, 1996. : - P. 214-218.469. Martin, C. W. Diaryldichlorocarbonyl ylides derived from dichlorocarbene and aromatic ketones[текст] / C.
W. Martin, H. S. Gill, J. A. Landgrebe // J. Org. Chem. - 1983. - V. 48. - № 11. - P. 18981901.470. Bors, D. A. Carbon acidity. 67. The indicator scale of cesium ion pairs in tetrahydrofuran [текст]/ D. A. Bors, M. J. Kaufman, A. Streitwieser // J. Am. Chem. Soc. - 1985. - V. 107. - № 24. - P. 69756982.471. Starflinger, W. Ene reaction mechanisms. 3. Intermolecular and intramolecular kinetic isotopeeffects (KIE) for some ene reactions of hetero enophiles [текст] / W. Starflinger, G.
Kresze, K. Huss// J. Org. Chem. - 1986. - V. 51. - № 1. - P. 37-40.472. Pinnick, H. W. Friedel-Crafts reactions of ethyl cyclopropanecarboxylate [текст] / H. W. Pinnick, S. P. Brown, E. A. McLean, L. W. Zoller // J. Org. Chem. - 1981. - V. 46. - № 18. - P. 37583760.473. Chen, Z.-K. New Phenyl-Substituted PPV Derivatives for Polymer Light-emitting DiodesSynthesis, Characterization and Structure-Property Relationship Study [текст] / Z.-K. Chen, N. H. S.Lee, W. Huang, V.-S. Xu, Y. Cap // Macromolecules.
- 2003. - V. 36. - № 4. - P. 1009-1020.474. Glende, C. Transformation of mutagenic aromatic amines into non-mutagenic species by alkylsubstituents: Part II: Alkylation far away from the amino function [текст] / C. Glende, M. Klein, H.Schmitt, L. Erdinger, G. Boche // Mutation Res. / Gen. Toxic. Env. Mut. - 2002. - V. 515.
- № 1-2. P. 15-38.475. Schmid, M. New C2v- and Chiral C2-Symmetric Olefin Polymerization Catalysts Based onNickel(II) and Palladium(II) Diimine Complexes Bearing 2,6-Diphenyl Aniline Moieties: Synthesis,Structural Characterization, and First Insight into Polymerization Properties [текст] / M. Schmid, R.Eberhardt, M. Klinga, M.
Leskela, B. Rieger // Organometallics. - 2001. - V. 20. - № 11. - P. 23212330.476. Zbruyev, A. I. Synthesis of polyarene derivatives of fused aziridines by Suzuki–Miyaura crosscoupling [текст] / A. I. Zbruyev, V. V. Vashchenko, A. A. Andryushchenko, S. M. Desenko, V. I.Musatov, I.
V. Knyazeva, V. A. Chebanov // Tetrahedronю - 2007. - V. 63. - № 20. - P. 4297-4303.404477. Braude, E. A. 624. Hydrogen transfer. Part XII. Dehydrogenation of "blocked" hydroaromaticcompounds by quinones [текст] / E. A. Braude, L. M. Jackman, R. P. Linstead, G. Lowe // J. Chem.Soc. - 1960. - P. 3123-3132.478.
Ranu, B. C. A New Redundant Rearrangement of Aromatic Ring Fused Cyclic βHydroxydithiane Derivatives. Synthesis of Aromatic Ring Fused Cyclic 1,2-Diketones with OneCarbon Ring Expansion [текст] / B. C. Ranu, U. Jana // J. Org. Chem. - 1999. - V. 64. - № 17, pp6380-6386.479. Bogert, M.
T. The Synthesis of Condensed Polynuclear Hydrocarbons by the Cyclodehydrationof Aromatic Alcohols. I. Indanes [текст] / M. T. Bogert, D. Davidson // J. Am. Chem. Soc. - 1934. V. 56. - № 1, pp 185-190.480. Tang, Y. Synthesis and characterization of chroman-containing compounds and their preliminaryassessment of cytotoxicity toward two human cancer cell lines [текст] / Y. Tang, J. Wei, W.
Zhong,X. Liu. // Heteroatom Chem. - 2010. - V. 21. - № 6. - P. 423-429.481. Stork, G. The Stereochemistry of the SN2' Reaction. I. Preparation of Pure trans-6-Alkyl-2cyclohexen-1-ols [текст] / G. Stork, W. N. White // J. Am. Chem. Soc. - 1956. - V. 78. - № 18. - P.4604-4608.482. Kuwabe, S. Palladium-Catalyzed Intramolecular C-O Bond Formation [текст] / S. Kuwabe, K.E. Torraca, S.
L. Buchwald // J. Am. Chem. Soc. - 2001. - V. 123. - № 49. - P. 12202-12206.483. Randall, J. C. A review of high resolution liquid13Carbon nuclear magnetic resonance chaarc-terizations of ethylene-based polymers [текст] / J. C. Randall // J. Macro. Sci. - Rev. Macro. Chem.Phys.
- 1989. - V. C29. - № 2-3. - P. 201-317.484. Tritto, I.13C NMR Studies of Ethylene-Propylene Copolymers Prepared with HomogeneousMetallocene-Based Ziegler-Natta Catalysts [текст] / I. Tritto, Z. Fan. - P. Iocatelli, M. Sacchi, I.Camurati, M. Galimberti // Macromolecules. - 1995. - V.
28. - № 9. - P. 3342-3350.485. Kakugo, M. Carbon-13 NMR determination of monomer sequence distribution in ethylenepropylene copolymers prepared with δ-titanium trichloride-diethylaluminum chloride [òåêñò] / M.Kakugo, Y. Naito, K. Mizunuma, T. Miyatake // Macromolecules. - 1982.
- V. 15. - № 4. - P. 11501152.405приложениеТаблица П1. Длины связей d [А] и величины углов ω [град] в соединении 1.21.1.21СвязьC(1)-C(5)C(1)-C(9)C(1)-C(2)C(2)-C(3)C(3)-C(4)C(3)-C(10)C(4)-C(5)C(4)-C(6)C(5)-C(8)C(6)-C(4а)C(6)-C(7)C(6)-C(7а)C(7)-C(8)C(8)-C(12)C(8)-C(11)d [А]1.364(2)1.495(2)1.507(2)1.509(2)1.340(2)1.493(2)1.458(2)1.509(2)1.508(2)1.509(2)1.564(2)1.564(2)1.555(2)1.529(2)1.532(2)УголC(5)-C(1)-C(9)C(5)-C(1)-C(2)C(9)-C(1)-C(2)C(1)-C(2)-C(3)C(4)-C(3)-C(10)C(4)-C(3)-C(2)C(10)-C(3)-C(2)C(3)-C(4)-C(5)C(3)-C(4)-C(6)C(5)-C(4)-C(6)C(1)-C(5)-C(4)C(1)-C(5)-C(8)C(4)-C(5)-C(8)C(4а)-C(6)-C(4)C(4а)-C(6)-C(7)C(4)-C(6)-C(7)C(4а)-C(6)-C(7а)C(4)-C(6)-C(7а)C(7)-C(6)-C(7а)C(8)-C(7)-C(6)C(5)-C(8)-C(12)C(5)-C(8)-C(11)C(12)-C(8)-C(11)C(5)-C(8)-C(7)C(12)-C(8)-C(7)C(11)-C(8)-C(7)ω [град]129.97(14)107.21(11)122.82(13)105.01(11)129.73(12)107.02(10)123.25(12)110.69(10)137.89(10)111.42(11)110.05(12)139.26(11)110.68(10)116.5(2)112.89(7)100.58(7)100.58(7)112.89(7)114.1(2)109.15(9)114.09(12)110.23(12)109.49(12)101.16(9)110.20(12)111.46(11)406приложениеТаблица П2.