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  • 1
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Following the studies on elucidating the main structural features of elementary units of polyphenylene-type polymers prepared by condensation of di- and monoacetylaromatic compounds, an X-ray structural analysis of 1,3,5-tris[4′-(C-o-carboranyl)biphenyl-4-yl]benzene (2) (systematic name: 1,3,5-tris[)1,2-dicarba-closo-dodecarborane(12)-1-yl(biphenyl-4-yl]benzene), which is the low-molecular-weight analog of one of the polymers in the given series, was performed. Compound 2 crystallizes as unstable solvate 1:1:1 with chloroform and benzene. The crystals are monoclinic, a = 17,060 Å, b = 20,220 Å, c = 18,448 Å, β = 102,79°, space group P21/n, Z = 4. Molecule 2 exhibits asymmetric conformation with substantial distortions of the linear geometry of polyphenylene units. The crystal is built of layers of molecules 2, the solvate molecules being situated between these molecules in the channels and cavities with a population of 2/3. The benzene molecules participate in stacking-interaction with one of the carboranyl-substituted (i.e., the strongest electron-acceptor) benzene rings of the host molecule 2; chloroform molecules pack the channels without a specific interaction with the host molecules.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: With the aim to determine the main structural characteristics of amorphous (branched and different-unit) polymers of the polyphenylene type, prepared by polycyclocondensation of carborane-containing mono- and diacetylaromatic compounds, an X-ray structural study of four model compounds was carried out, viz. of 1,2-bis[4-(4-acetylphenoxy)phenyl]-1,2-dicarba-closo-dodecaborane(12) (1) (triclinic crystals, a = 8,205 Å, b = 13,505 Å, c = 14,019 Å, α = 90,44°, β = 97,08°, γ = 97,24°, space group P1, Z = 2, R = 0,045 for 2663 reflections), 1,2-bis(4-phenoxyphenyl)-1,2-dicarba-closo-dodecaborane(12) (2) (monoclinic crystals, a = 14,813 Å, b = 17,133 Å, c = 11,211 Å, β = 112,43°, space group P21/c, Z = 4, R = 0,066 for 3 286 reflections), 1,2-bis(4′-acetylbiphenyl-4-yl)-1,2-dicarba-closo-dodecaborane(12) (3) (orthorhombic crystals, at -120°C a = 13,405 Å, b = 9,276 Å, c = 22,86 Å, space group Pnam, Z = 4 molecules on the m plane, R = 0,039 for 1 147 reflections), and 1,2-bis(4-acetylbenzyl)-1,2-dicarba-closo-dodecaborane(12) (4) (orthorhombic crystals, at -120°C a = 22,03 Å, b = 26,23 Å, c = 8,026 Å, space group Fdd2, Z = 8 molecules lie on the two-fold axis, R = 0,051 for 577 reflections). The strained structure of the C,C′-o-diphenyl-substituted carboranyl fragment is established, the high conformational flexibility of 4-phenoxyphenyl linkages is confirmed and a tendency toward separate autoassociation of acetyl-containing polar groups and carborane nuclei is shown, with the autoassociation of polar groups completely suppressing that of carborane nuclei in case of conformational rigidity and shortness of the arylene linkages. These and other structural characteristics of the investigated model compounds and their crystals, in case they turn out to be characteristic also for the corresponding polymers and their precursors, should largely determine the structure and physico-chemical properties of their corresponding polymers.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The structure of a number of polymers of the polyphenylene type, prepared by polycyclocondensation of aromatic diketones and their acetals was investigated by 13C NMR spectroscopy. The spectra provide a means to determine the content of 1,3,5-trisubstituted benzene rings and defective β-methylchalcone fragments, as well as the endgroups.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: For elucidating the structural features of elementary units of polyphenylene type polymers, prepared by polycondensation of di- and mono-acetylaromatic compounds, and X-ray study of two model compounds was performed, viz. 1,3,5-tris(4-biphenylyl)benzene (1) and 1,3,5-tris[4-(C-o- carboranylmethyl)phenyl]benzene (2) (diffractometer: R = 0,063 (1) and 0,061 (2))· 1 0,5 C6H6 crystals were found to be rhombohedral, a = 20,168 (3), c = 13,678 (3) Ǎ, space group R3c, Z = 6;2· CHCl3 crystals are triclinic, a = 15,7528 (2), b = 12,7004 (6), c = 15,460 (2) Å, α = 109,97(1) β = 111,92(1) γ = 100,69 (2) °, space group P1, Z = 2. In the crystal the molecule 1 has a 32 symmetry with a propeller-like orientation of the biphenyl fragments with respect to the central ring (the rotation of the disubstituted benzene rings relative to the central one is 47,2° and relative to the therminal ones, it is 35,9°). In2 the disubstituted benzene rings are rotated with respect to the central one by different values (dihedral angeles are 31,7 - 30,7, and 52,5°). In all benzene rings of both molecules a decrease of the endocyclic bond angles at the ipso-atoms is observed which in 2 depends on the dihedral angeles between the planes of bonded benzene rings. All there carboranylmethylphenyl fragements in 2 have the same conformation: the CH-group of the carborane skeleton “hangs” over the benzene ring plane. The crystal packing of 1and 2 is characterized by sufficiently large cavities which are occupied by solvent molecules. In crystals of 2 the carborane parts of the molecules are associated into separate structural motives.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Carborane-containing oligoorganosilazanes (COS) (20 to 60 wt.-%) prepared by coammonolysis of (o-carboranylmethoxy)dichloro(phenyl)silane and trichloro(phenyl)silane (COS 1), or 1-chloro-1-phenyl-1-sila-2,7-dioxa-4,5-(1,2-carborano)cycloheptane and dichloro(dimethyl)-silane (COS 2), were used to crosslink polyphenylene type prepolymers on the basis of 4,4′-oxydiacetophenone and acetophenone (FPP-1). This allowed the reduction of the crosslinking temperature of FPP-1 by 100-150°C, retaining a high heat resistance of the final crosslinked polymer. Octamethylcyclotetrasilazane (15 wt.-%) was used to crosslink the carborane-containing prepolymers on the basis of 1,2-bis[4-(4-acetylphenoxy)phenyl]-o-carborane and acetophenone (FPP-2) and 1,2-bis(4-acetylbenzyl)-o-carborane and acetophenone (FPP-3). At 350°C a polymer was formed with a gel fraction amounting to 94%.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Crosslinking reactions of prepolymers of the polyphenylene type carrying acetyl end-groups, based on 4,4′-oxydiacetophenone and acetophenone (FPP-1), or 4-acetylacetophenone and 4-(4-acetylphenoxy)phenyl-o-carborane (FPP-2), by means of 20-80 wt.-% of 1,2-bis[hydrido-(dimethyl)siloxymethyl]-o-carborane (1) were investigated. It was found that the prepolymer FPP-1 is easily crosslinked in the presence of 30 wt.-% of 1 at 300°C, and the prepolymer FPP-2 at 350°C.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: New mono- and bifunctional isopropenyl derivatives of o-carborane were synthesized according to the Witting reaction, from the corresponding acetyl derivatives and methylenetriphenylphosphorane. The radical copolymerization with methyl methacrylate was investigated and thermal and thermomechanical characteristics of the obtained copolymers were studied. In copolymers prepared on the basis of a monofunctional carborane-containing monomer, the increase of glass transition temperature takes practically a linear course with increasing boron content. In crosslinked copolymers the presence of o-carborane fragments leads to the widening of the glass transition temperature range, predominantly at low temperatures, irrespective of the type of bifunctional monomer used.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 1973-1979 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The synthesis, crystal structure and detatiled molecular mechanics calculations, including crystal packing interactions, of tetrahexylsubstituted sexithienylene are presented. Unexpectedly the molecule, which arranges in the P-1 space group, displays no herringbone arrangement, thienylenic rings are far from coplanarity and the alkylic side chains present different conformations. Molecular mechanics fully accounts for these findings. From crystal packing computations it is derived that different arrangements are unable to lower the packing energy, due to the closeness of two alkyl chains on the same side of the thienylenic backbone, which prevents interspersion of non-parallel molecules.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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