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侧链含锑聚硅烷的合成与性能研究 被引量:6

Synthesis and Characterization of Polysilanes with Antimony Side Groups
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摘要 侧链含锑聚硅烷的合成可通过聚甲基硅烷的高分子反应在室温条件下实现,聚合物产率为75.2%,数均分子量为1600。其分子结构与组成可由元素分析、FT-IR、^1H—NMR、^29Si CP/MAS NMR、GPC和UV来确认。PSA可溶于一般常见的有机溶剂,紫外吸收的最大波长为330nm,其热分解特性表明,陶瓷收率为80%,可用作SiC陶瓷先驱体;其本体电导率为10^-8~10^-7S/cm,将其与碘掺杂,电导率可以达到10^-5S/cm以上。 Polysilanes with antimony side groups (PSA) can be synthesized from polymer reaction of polymethylsilane at room temperature. In so doing, the yield of polymer is 75.2% and the average molecular weights of the polymer are around 1600. Its chemical composition and structure can be characterized by elemental analysis, FF-IR, 1H-NMR,^29Si CP/MAS NMR, GPC, and UV. It is soluble in the common organic solvent; the UV absorption maximum wavelength is 330urn. The property of pyrolysis shows that its ceramic yield is 80% and it is a potential preceramic polymer. This polymer shows good semiconductive properties, whose intrinsic conductivities are within the range of 10^-8~ 10^-7S/cm, and can be increased above 10^5 S/cm after being doped with iodine.
出处 《国防科技大学学报》 EI CAS CSCD 北大核心 2008年第3期15-20,共6页 Journal of National University of Defense Technology
基金 国家部委资助项目(51310060101)
关键词 聚硅烷 聚甲基硅烷 高分子反应 含锑侧基 半导体性能 polysilanes polymethylsilane polymer reaction antimony side groups semiconductive properties
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参考文献11

  • 1Miner R D, Michl J. Polysilane High Polymers [J]. Chem. Rev., 1989, 89(6): 1359- 1410.
  • 2Brook M A. Silicon in Organic, Organometallic, and Polymer Chemistry [M]. New York: A Wiley-Interseience Publication, 2000: 352.
  • 3Acharya A, Seki S, Saeki A, et al. Polysilanes with Functional Groups [J]. Synthetic Metals, 2006, 156(2-4): 293 -297.
  • 4Sacarescu L, Ardeleanu R, Sacarescu G, et al. Trends in Organometallic Chemistry Research [M]. Nova Science Publishers, Hauppauge, 2005: 85- 106.
  • 5Stuger H, West R. Polysilane High Polymers with Olefinic Side Groups: Syntheses, Properties and Addition Reactions [J]. Macroraolecules, 1985, 18:2349 - 2354.
  • 6Amberger E, Salazar R W G. Mixed Organometallic Compounds of Group Ⅵ : Synthesis of Tris(Trimethyl-group-Ⅳ) Stibines [J]. J. Organomet. Chem., 1967,8(1): 111-114.
  • 7Schulz S, Nieger M. Reactivity of Aluminum Trialkyls R3Al, Diorganoaluminum Chlorides R2AlCl (R= Me, Et, t-Bu), and Me2AlH toward Sb (SiMe3)3[J]. Organomet., 1999, 18W:315-319.
  • 8Fukushima M, Tabei E, Aramata M. Elect.el, Conductivity of Organosilicon Polymers Ⅱ: Synthesis and Electrical Conductivities of Iodine-doped Polysilanes Containing Amino Groups [J]. Synthetic Metals, 1998, 96(2- 4): 245- 248.
  • 9邢欣,李效东,郭爱青,曹峰,王军.聚甲基硅烷的合成与封端[J].高分子学报,2004,14(5):705-708. 被引量:4
  • 10Cotton F A, Wilkinson G. Advanced Inorganic Chemistry [M]. New York: Wiley-interscience, 1988: 390.

二级参考文献12

  • 1Scarlete M,Brienne S,Butler I S,Harrod J F.Chem Mater, 1994,6:977 - 982
  • 2Matyjiaszewski K. Polym Prepr,1990,31(2) :224- 229
  • 3Miller R D, Michl J. Chem Rev, 1989,89(6): 1359 - 1410
  • 4Gozzi M F,Yoshida I V.Eur Polym J,1997,33(8):1301 - 1306
  • 5Masaki N,Satoshi O,Takashi I,Kiyohito O,Kunio O,Takaaki D. Journal of the Ceramic Society of Japan,1998,106(2):220 - 223
  • 6Masaki N,Takeshi Y,Takashi I,Yoshiro K,Kiyohito O,Kunio O,Takaaki D.Chem Mater,2000,12:2686- 2692
  • 7Hurwitz F I, Kacik T A, Bu X Y, Masnovi J, Heimann P J, Beyene K. J Mater Sci, 1995,30: 3130 - 3136
  • 8Zhang Z F, Scotto C S, Laine R M. J Mater Chem, 1998,8: 2715 - 2724
  • 9Seyferth D.Timothy G,Henry J.J Am Ceram Soc, 1992,75(5):1300 - 1302
  • 10Boury B,Bryson N,Soula G.Appl Organometal Chem,1999,13 :419 - 430

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