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1Academic Journal
مصطلحات موضوعية: 键级守恒, NiCu(100), 甲烷化反应, 积碳效应, bond-order conservation, methanation reaction, deposited carbon eFFect
Relation: 化学学报,1998,(8):47-53; HXXB199808007; http://dspace.xmu.edu.cn/handle/2288/107496
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2Report
المؤلفون: 陸大榮
المساهمون: 行政院國家科學委員會, 國立中興大學化學系(所)
مصطلحات موضوعية: 化學類, 基礎研究, asymmetric synthesis, 不對稱合成, 立體選擇性, 樟腦, 亞胺內酯, 親核性甘胺酸根, 烷化反應, ?-胺基酸, 相轉移催化劑, 氰醇化反應, 醛醇反應, 2-胺基醇, 四氫.咯, stereoselectivity, camphor, iminolactone, glycinate, alkylation,?-amino acid, phase transfer catalyst, cyanohydrin formation, camphoramic acid, ?-aminoalcohol,pyrrolidine
Time: 1
Relation: http://grbsearch.stpi.narl.org.tw/GRB/result.jsp?id=1415766& plan_no=NSC96-2113-M005-005-MY3& plan_year=96& projkey=PA9607-0479& target=plan& highStr=*& check=0& pnchDesc=%E6%96%B0%E4%B8%8D%E5%B0%8D%E7%A8%B1%E5%90%88%E6%88%90%E6%96%B9%E6%B3%95%E4%B9%8B%E7%A0%94%E7%A9%B6; NSC96-2113-M005-005-MY3; http://hdl.handle.net/11455/49447
الاتاحة: http://hdl.handle.net/11455/49447
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3Academic Journal
Relation: http://repository.ust.hk/ir/Record/1783.1-107834; 華東理工大學學報, v. 1997, (05), 1997
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4
المؤلفون: 梁家榮, Chia-Jung Liang
المساهمون: 葉名倉, Ming-Chang P. Yeh
مصطلحات موضوعية: 螺旋化合物, 環氧化反應, 內酯化反應, 三氯化鐵, 環丙烷化反應, 擴環反應, 六氫吲哚, 金催化反應, 克萊森重排反應, 三鹵化銦, 炔醯胺化合物, 胺基茚化合物, 茚并吡啶化合物, spiro compound, epoxidation, lactonization, iron(III) chloride, cyclopropanation, ring expansion reaction, hexahydroindole, gold(I) catalyzed, Claisen rearrangement, indium(III) halide, ynamide, aminoindene, indeno[2, 1-b]pyridine
Relation: GN080042014S; http://etds.lib.ntnu.edu.tw/cgi-bin/gs32/gsweb.cgi?o=dstdcdr&s=id=%22GN080042014S%22.&%22.id.&; http://rportal.lib.ntnu.edu.tw:80/handle/20.500.12235/100992
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5
المؤلفون: 李懿祐, Li, Yi-You
المساهمون: 李位仁, Lee, Way-Zen
مصطلحات موضوعية: 四價錳錯合物, 硫醇基烷化反應, Manganese(IV) complexes, Thiolate alkylation
Relation: G060542072S; http://etds.lib.ntnu.edu.tw/cgi-bin/gs32/gsweb.cgi?o=dstdcdr&s=id=%22G060542072S%22.&%22.id.&; http://rportal.lib.ntnu.edu.tw:80/handle/20.500.12235/100217
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6Dissertation/ Thesis
المؤلفون: Bi-Hung Juang, 莊必泓
المساهمون: 化學工程學系所, 楊鴻銘, Hung-Ming Yang
مصطلحات موضوعية: Phase transfer catalyst, solid-liquid system, succinimide, ultrasound, N-alkylation, 相間轉移觸媒, 固-液相, 琥珀醯亞胺, 超音波, 氮烷化反應
Relation: U0005-2006201416163000; http://hdl.handle.net/11455/91532
الاتاحة: http://hdl.handle.net/11455/91532
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7
المؤلفون: 張惟盛, Chang, Wei-Sheng
المساهمون: 淡江大學化學工程與材料工程學系碩士班, 陳錫仁
مصطلحات موضوعية: 煤炭氣化複循環發電, 化學遷移反應, 甲烷化反應, 合成氣, 合成天然氣, 程序最適化, Integrated Gasification Combined Cycle (IGCC), Shift Reactions, Methanation, Syngas, Synthetic natural-gas (SNG), Process Optimization
Relation: [1] 鍾丁茂，碳排放減量與京都議定書，生態台灣季刊，8期，第42-44頁 (2005) [2] 許哲維，煤炭氣化複循環發電系統之整合設計暨其應用，碩士論文，淡江大學，台北 (2008) [3] 陳維新，化石燃料與空氣污染，海洋大學輪機系網頁，http://ind.ntou.edu.tw/~metex/ [4] 煤，Baidu百科，http://baike.baidu.com/view/23985.htm [5] 李文伯，高效率低汙染淨煤發電技術-IGCC，經濟部能源局能源報導，第5頁 (2007) [6] 姚強，21世紀可持續能源技術-潔淨煤技術，化學工業出版社，第23-218頁 (2005)。 [7] 郭樹才，煤化工工藝學，化學工業出版社，第222-233頁 (1997) [8] Apt, J., A. Newcomer, L. B. Lave, S. Douglas, L. M. Dunn, “An Engineering-Economic Analysis of Syngas Storage,” National Energy Technology Laboratory, U.S.A. (2008) [9] Hu, D., J. Gao, Y. Ping, L. Jia, P. Gunawan, Z. Zhong, G. Xu, F. Gu, and F. Su, “Enhanced Investigation of CO Methanation over Ni/Al2O3 Catalysts for Synthetic Natural Gas Production,” Ind. Eng. Chem. Res., 51, 4875-4886 (2012) [10] Razzaq, R., H. Zhu, L. Jiang, U. Muhammad, C. Li, and S. Zhang, “Catalytic Methanation of CO and CO2 in Coke Oven Gas over Ni-CO/ZrO2-CeO2,” Ind. Eng. Chem. Res., 52, 2247-2256 (2013) [11] Seider, W. D., J. D. Seader, D. R. Lewin, and S. Widagdo, “Product and Process Design Principles Synehesis, Analysis and Evaluation,” third ed, John Wiley & Sons. Inc., Hoboken, N. J. (2010) [12] Smith, R., “Chemical Process Design and Integration,” 2nd th, John Wiley & Sons Ltd., West Sussex, U. K. (2005) [13] AspenPlus, ASPEN PLUS User’s Guide, version 7.3, Aspen Tech., Boston, MA, U.S.A. (2011). [14] AspenPlus, Physical Property Methods and Models Reference Manual, Aspen Tech., Boston, MA, U.S.A. (2006). [15] Aspen Technology, Inc., “Rate-Based Model of the CO2 Capture Process by MEOH using Aspen Plus” (2008) [16] Gross, J., and G. Sadowski, “Perturbed-Chain SAFT：An Equation of State Based on a Perturbation Theory for Chain Molecules,” Ind. Eng. Chem. Res., 40, 1244-1260 (2001) [17] Amra, T., “Group Contribution sPC-SAFT Equation of State, ” Ph.D. Thesis, Technical University of Denmark, Denmark [18] Bhattacharyya, D., R. Turton, and S. E. zitney, “Steady-State Simulation and Optimization of an Integrated Gasification Combined Cycle Power Plant with CO2 Capture,” Ind. Eng. Chem. Res., 50, 1674-1690 (2011); U0002-0506201316343800; http://tkuir.lib.tku.edu.tw:8080/dspace/handle/987654321/94372; http://tkuir.lib.tku.edu.tw:8080/dspace/bitstream/987654321/94372/-1/index.html
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8Dissertation/ Thesis
المؤلفون: 陳冠霖, Chen, Kuan-Lin
المساهمون: 化學工程學系所, 楊鴻銘, Hung-Ming Yang
مصطلحات موضوعية: 相間轉移觸媒, Phase – transfer catalyst, 固-液相, 琥珀醯亞胺, 氮烷化反應, Solid – liquid phase, succinimide, N-alkylation
Relation: http://www.airitilibrary.com/Publication/alDetailedMesh1?DocID=U0005-2606201320545900; U0005-2606201320545900; http://hdl.handle.net/11455/3170
الاتاحة: http://hdl.handle.net/11455/3170
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9Dissertation/ Thesis
المؤلفون: 李伯东
المساهمون: 袁友珠
مصطلحات موضوعية: CNT, glycerol hydrogenolysis, CO-PROX, CO selectivity methanation, 碳纳米管, 甘油氢解反应, CO优先氧化反应, CO选择甲烷化反应
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10Dissertation/ Thesis
المساهمون: 應用化學系碩博士班
مصطلحات موضوعية: 甲烷化反應, 催化劑, 二氧化碳, methanation, carbon dioxide, catalyst, nickel
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11
المؤلفون: 吳晨帆, Chen-Fan Wu
المساهمون: 劉行讓博士, Dr. Hsing-Jang Liu
مصطلحات موضوعية: 脂肪分解酵素, 芳香基環己醇, 掌性α-氰基酯化合物, 烷化反應, Lipase AK, ( + )-2-Arylcyclohexanols, (-)-2-Arylcyclohexanols, Chiral Auxilaries, Asymmetric Alkylation, a-Cyano Esters, Kinetic Resolution
Time: 31
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12Dissertation/ Thesis
المؤلفون: 施朝仁, Shih, Chao-Jen
المساهمون: 賴美津, 中興大學, 顏宏真, 黃介辰, 吳韋訥, 黃啟裕
مصطلحات موضوعية: 鹽逆境適應, Salt-stress response, 差異性表現反轉錄聚合酶連鎖反應, 高鹽甲烷太古生物, 分子伴護蛋白ClpB, 廣泛逆境蛋白USPA, 甲烷化反應, 緊迫反應, 太古生物, 高鹽甲烷, 逆境反應, Salt-stress adaptation, Differential display reverse transcription-PCR (DDRT-PCR), Halophilic methanogen, Molecular chaperone ClpB, Universal stress protein USPA, Methanogenesis, Strigent response, Archaea, chaperone, Methanohalophilus, Stress response
Relation: http://www.airitilibrary.com/Publication/alDetailedMesh1?DocID=U0005-1708200714361000; U0005-1708200714361000; http://hdl.handle.net/11455/22535
الاتاحة: http://hdl.handle.net/11455/22535
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13Dissertation/ Thesis
المؤلفون: 陳婉怡, W. Y. Chen
المساهمون: 陳阿煌, Arh-Hwang Chen
مصطلحات موضوعية: 不對稱合成, 掌性輔助劑, 掌性催化劑, 消旋化, 烷化反應, chiral auxiliaries, chiral catalyst, racemization, alkylation
وصف الملف: 110 bytes; text/html
Relation: http://ir.nknu.edu.tw/ir/handle/987654321/1521; http://ir.nknu.edu.tw/ir/bitstream/987654321/1521/1/index.html
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14
المؤلفون: 郭俊徹, Jiunn-Cheh Guo
المساهمون: 劉行讓, Hsing-Jang Liu
مصطلحات موضوعية: α-氰基丙烯酸酯, 還原去氰烷化反應, 還原去氰1,4-加成反應, 螺旋狀化合物, α-Cyanoacrylates, reductive decyanation alkylation, reductive decyanation 1,4-addition, spiro compounds
Time: 31
وصف الملف: 155 bytes; text/html
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(b) Chanon, M.；Tobe, M. L. Angew. Chem., Int. Ed. Engl. 1982, 21, 1. (c) Pross, A. Acc. Chem. Res. 1985, 18, 212. (d) Chanon, M. Acc. Chem. Res. 1987, 201, 214. 15. (a) Harring, S. R.；Livinghouse, T. Tetrahedron Lett. 1989, 30, 1499. (b) Barluenga, J.；Fernandez-Simon, J. L.；Concellon, J. M.；Yus, M. Synthesis 1988, 234. (c) Komatsu, K.；Nishinaga, T.；Aonuma, S.；Hirosawa, C.；Takeuchi, K.；Lindner, H. J.；Richter, J. Tetrahedron Lett. 1991, 32, 6767. (d) Kondo, Y.；Muraata, N.；Sakamoto, T. Heterocycles 1994, 37, 1467. (e) Guijaro, A.；Yus, M. Tetrahedron 1994, 50, 13269. (f) Guijaro, A.；Romon, D. J.；Yus, M. Tetrahedron 1993, 49, 469. 16. Guijaro, A.；Yus, M. Tetrahedron 1994, 50, 3447. 17. Agawa, T.；Ishida, M.；Ohshiro, Y. Synthesis 1980, 933. 18. Pradhan, S. K.；Radhakrishnan, T. V.；Subramanian, R. J. Org. Chem. 1976, 41, 1943. 19. (a) Bartmann, E. Angew. Chem., Int. Ed. Engl. 1986, 25, 653. (b) Almena, J.；Foubeo, F.；Yus, M. J. Org. Chem. 1994, 59, 3210. 20. Clive, D. L. J.；Keshava, Myrthy, K. S.；Zhang, C.；Hayward, W. D.；Daigneault, S. J. Chem. Soc., Chem. Commun. 1990, 509. 21. Philips, K. D.；Horwitz, J. P. J. Org. Chem. 1975, 40, 1856. 22. (a) Rieke, R. D.；Dawson, B. T.；Stack, D. E.；Stinn, D. E. Synth. Commun. 1990, 20, 2711. (b) Jutzi, P.；Hielscher, B. Organometallics 1986, 5, 1201. 23. (a) Rychnovsky, S. D.；Swenson, S. S. J. Org. Chem. 1997, 62, 1333. (b) Malassene, R.；Vanquelef, E.；Toupet, L.；Hurvois, J. P.；Moinet, C. Org. Biomol. Chem. 2003, 1, 547. (c) Savoia, D.；Taglivini, E.；Trombini, C.；Umani-Ronchi, A. J. Org. Chem. 1980, 45, 3227. (d) Shono, T.；Terauchi, J.；Kitayama, K.；Takeshima, Y. I.；Matsumura, Y. Tetrahedron 1992, 48, 8253. (e) Kang, H. Y.；Hong, W. S.；Cho, Y. S.；Koh, H. Y. Tetrahedron Lett. 1995, 36, 7661. (f) Black, D. St. C.；Doyle, J. E. Aust. J. Chem. 1978, 31, 2323. (g) E. E. van Tamelen,；Bjorklund, C.；Rudler, H. J. Am. Chem. Soc. 1971, 93, 7113. 24. Shia, K. S.；Chang, N. Y.；Yip, J.；Liu, H. J. Tetrahedron Lett. 1997, 38, 7713. 25. Liu, H. J.；Shia, K. S.；Zhu, J. L. Tetrahedron Lett. 1998, 39, 4183. 26. 戴嘉良，碩士論文，國立清華大學，1999年. 27. 謝琬萍，碩士論文，國立清華大學，2001年. 28. Liu, H. J.；Ly, T. W.；Tai, C. L.；Wu, J. D.；Ling, J. K.；Guo, J. C.；Tseng, N. W.；Shia, K. S. Tetrahedron 2003, 59, 1209. 29. (a) Huang, M. J. Am. Chem. Soc. 1946, 68, 2487. (b) Huang, M. J. Am. Chem. Soc. 1949, 71, 3301. 30. Liu, H. J.；Tsai, T. Y.；Shia, K. S. Synlett 2003, 1, 97. 31. 蔡廷岳，博士論文，國立清華大學，2004年. 32. 曹景博，博士論文，國立清華大學，2005年. 33. For leading references, see (a) Fleming, I.；Barbero, A.；Walter, D. Chem. Rev. 1997, 97, 2063. (b) van Staden, L.F.；Gravestork, D.；Anger, D. Chem. Soc. Rev. 2002, 31, 195. 34. Kocienski, P. Chem. Ind. (London) 1981. 548. 35. Julia, M.；Paris, J. M. Tetrahedron Lett. 1973, 4833. 36. Prajapati, D.；Lekhok, K. C.；Sandhu, T. S.；Ghosh, A. C. J. Chem. Soc., Perkin Trans. 1 1996, 1. 37. Rapoport, H.；Campion, J. E. J. Am. Chem. Soc. 1951, 73, 2239. 38. Charlton, M. A.；Green, J. R. Can. J. Chem. 1997, 75, 965. 39. Christensen, S. B.；Guider, A.；Forster, C. J.；Gleason, J. G.；Bender, P. E.；Karpinski, J. M.；DeWolf, Jr. W. E.；Barnette, M. S.；Underwood, D. C.；Griswold, D. E.；Cieslinski, L. B.；Burman, M.；Bochnowicz , S.；Osborn, R. R.；Manning, C. D.；Grous, M.；Hillegas, L. M. ；Bartus, J. O.；Ryan, M.D.；Eggleston, D. S.；Haltiwanger, R. C.；Torphy, T. J. J. Med. Chem. 1998, 41, 821-835. 40. Yoshida, Y.；Hayashi, R.；Sumihara, H.；Tanabe, Y. Tetrahedron Lett. 1997, 38, 8727. 41. Paquette, L. A.；Wang, H. L. J. Org. Chem. 1996, 61, 5352. 42. Erickson, K. L. in Marine Natural Products；Scheuer, P. J., Ed.；Academic Press：New York, 1983；Vol. 5, pp 131. 43. Iwata, C.；Miyashita, K.；Koga, Y.；Shinoo, Y.；Yamada, M.；Tanaka, T. Chem. Pharm. Bull. 1983, 31, 2308. 44. (a) Wolinsky, L. E.；Faulkner, D. J. J. Org. Chem. 1976, 41, 597. (b) Ichinose, I.；Kato, T. Chem. Lett. 1978, 61. 45. Martin, J. D.；Perez, C.；Ravelo, J. L. J. Am. Chem. Soc. 1986, 108, 7801. 46.Iwata, C.；Akiyama, T.；Miyashita, K. Chem. Pharm. Bull. 1988, 36, 2872. 47. Fenical, W. J. Phycol. 1975, 11, 245. 48 Faulkner, D. J. Pure Appl. Chem. 1976, 48, 25. 49. Gonzalez, A. G.；Aguiar, J. M.；Martin, J. D.；Norte, M. Tetrahedron Lett. 1975, 2499. 50. (a) Suzuki, M.；Kurosawa, E. Tetrahedron Lett. 1978, 4805. (b) Suzuki, M.；Furusaki, A.；Hashiba, N.；Kurosawa, E. Tetrahedron Lett. 1979, 879. 51. Niwa, H.；Yoshida, Y.；Hasegawa, T.；Yamada, K. Chem. Lett. 1985, 1687. 52. Niwa, H.；Yoshida, Y.；Hasegawa, T.；Yamada, K. Tetrahedron 1991, 47, 2155. 53. (a) Rinehart, R. E.；Lasky, J. S. J. Am. Chem. Soc. 1964, 86, 2516. (b) Boulin, B.；Arreguy-Sun Miguel, B.；Delmond, B. Tetrahedron 2000, 56, 3927. 54. Dratch, S.；Charnikhova, T.；Saraber, F. C. E.；Jansen, B. J. M.；De Groot, A. Tetrahedron 2003, 59, 4287. 55. Chakravarty, A. K.；Das, B.；Mukhopadhyay, S. Tetrahedron 1991, 47, 2337. 56. Kircher, H. W.；Rosenstein, F. U. J. Org. Chem. 1987, 52, 2586. 57. Shiina, I.；Suzuki, M.；Yokoyama, K. Tetrahedron Lett. 2004, 45, 965. 58. Lam, T.；Ling, T.；Chowdhury, C.；Chao, T. H.；Bahjat, F. R.；Lloyd, G. K.；Moldawer, L. L.；Palladino, M. A.；Theodorakis, E. A. Bioorg. Med. Chem. Lett. 2003, 13, 3217. 59. Paquette, L. A.；Kang, H.-J. J. Am. Chem. Soc. 1991, 113, 2610.; http://nthur.lib.nthu.edu.tw/dspace/handle/987654321/30393
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15Dissertation/ Thesis
المؤلفون: 張家豪, Chang, Chia-Hao
المساهمون: 楊台鴻, 臺灣大學：高分子科學與工程學研究所
مصطلحات موضوعية: 小腦顆粒型神經細胞, 聚四氟乙烯, 丁基鋰, 推電子溶劑, 親疏水性, 細胞圖案, 微流道, 去氟反應, 烷化反應, cerebellum cortical granule cells, polytetrafluoroethene, butyllithium, electron-donating solvent, hydrophobicity, cellular pattern, microfluidic channel, defluorination, alkylation
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Relation: 1. Ravi Bellamkonda, Patrick Aebischer, “Review：tissue engineering in the nervous system,” Biotechnol. bioeng, 43(1994), 543-554 2. Chen Y.S., Hsieh C.L., Tsai C.C., Chen T.H., Cheng W.C., Hu C.L., Yao C.H., “Peripheral nerve regeneration using silicone rubber chambers filled with collagen, laminin, & fibronectin,” Biomaterials, 21(2000), 1541-1547 3. Woerly S., Morassutti D.J., “New aspects of neuroplantation,” Neurosurg Rev., 16(1993), 93-104 4. Gerald Karp, “Cell and molecular biology,” John Wiley and Sons, Inc. New York, USA, (2002) 5. Vellamkonda R., Raneri J.P., Bouche N., Arbischer P., “Hydrogel -based three-dimensional matrix for neural cell,” J. Biomed. Mater. Res., 29(1995), 663-671 6. Aebischer P., Valentini R.F., Dario P., Domenici C., Galletti P.M., “Piezoelectric guidance channels enhance regeneration in the mouse sciatic nerve after axotomy,” Brain Res., 436(1987),165-168 7. Dunnen W.F.A., Lei B.V.D., Schakenraad J.M., Stokroos I., Pennings A.J., Robinson P.H., “Long-term evaluation of nerve regeneration in a biodegradable nerve guide,” Microsurg., 14(1993), 508-515 8. Borkenhagen M., Stoll R.C., Neuenschwander P., Suter U.W., Aebischer P., “In vivo performance of a new biodegradable polyester urethane system used as a nerve guidance channel,” Biomaterials, 19(1998), 2155-2165 9. Woerly S., Marchand R., “Intracerebral implantation of synthetic polymer/biopolymer matrix: a new perspective for brain repair,” Biomaterials, 11(1990), 97-107 10. Harsch J. Calderon R.B., Timmons G.W., “Pulsed plasma deposition of allyamine on polysiloxane: a stable surface for neuronal cell adhesion,” J. Neurosci. Meth. 98(2000), 135-144 11. R. F. Valentini, A. M. Sabatini, P. Dario, P. Aebischer, “Polymer electret guidance channels enhance peripheral nerve regeneration in mice,” Brain res., 480(1989), 300-304 12. Sergio Martinoia, Marco Bove, Mariateresa Tedesco, Benno Margesin, Massimo Grattarola, “A simple microfluidic system for patterning populations of neurons on silicon micromachined substrates,” J. neurosci. methods, 87(1999), 35-44 13. Milan Mrksich, Laura E. Dike, Joe Tien, Donald E. Ingber, George M. Whitesides, ”Using microcontact printing to pattern the attachment of mammalian cells to self-assembled monolayers of alkanethiolates on transparent films of gold and silver,” Exp. cell res., 235(1997), 305-313 14. Zhang S, Yan L, Altman M, Lassle M, Nugent H, Frankel F, Lauffenburger DA, Whitesides GM, Rich A., “Biological surface engineering: a simple system for cell pattern formation,” Biomaterials, 20(1999), 1213-1220 15. Degenaar P, Pioufle BL, Griscom L, Tixier A, Akagi Y, Morita Y, Murakami Y, Yokoyama K, Fujita H, Tamiya E., “A method for micrometer resolution patterning of primary culture neurons for SPM analysis,” J.Biochem. 130(2001), 367-376 16. Hirokazu Kaji, Kazuto Tsukidate, Tomokazu Matsue, and Matsuhiko Nishizawa,, “In Situ Control of Cellular Growth and Migration on Substrates Using Microelectrodes,” J. AM. CHEM. SOC., 126(2004), 15026-15027 17. Charles E. Carraher, Jr. ”Polymer Chemistry,” Marcel Dekker, Inc., New York, (2000) 18. Jiri Jansta, Frantisek P. Dousek, ”Electrochemical corrosion of polytetrafluorethylene contacting lithium amalgam,” Electrochim. acta., 18(1973) 673-674 19. J. Jansta, F.P. Dousek, J.Riha, J.Heyrovsky, “Quantitative explanation of the mechanism of corrosion of poly(tetrafluoroethylene) caused by active alkali metals,” J. appl. polym. sci., 19(1975), 3201-3210 20. Ladislav Kavan, Zdenek Bastl, Frantisek P. Dousek, Jiri Jansta, “XPS study of carbon in electrochemical reduction products of poly(tetrafluoroethylene),” Carbon, 22(1984), 77-81 21. L. KAVAN, P. JANDA, J. WEBER, “Surface modification of poly(tetrafluoroethylene) by magnesium amalgam,” J. mater. sci., 36(2001), 879-885 22. Yasuhiro Okuda, Fumihiro Hayashi, Hiroshi Sakurai, Masaru Shiotani, ”A spectroscopic study on defluorination of poly (tetrafluoroethylene) by alkyllithium/electron-donating solvents,” Spectrochim. Acta. Part A. 60(2004) 3071-3077 23. Jaromir Hlavaty, Ladislav Kavan, Zdenek Bastl, “Stimultaneous fluorine elimination and alkylation of poly(tetrafluoroethylene) ,” Angew. Macrom. Chem. 238(1996) 165-175 24. Thomas A. Zwier, Michael F. Burke, “Chemical Modification of a Carbon Adsorbent for Liquid Chromatography, “Anal. Chern., (53)1981, 812-816 25. Anthony J. Dias and Thomas J. McCarthy, “Surface Modification of Poly(chlorotrifluoroethy1ene) with Methyllithium,” Macromolecules, 18(1985), 1826-1829 26. Nilanjan Chakrabarti, John Jacobus, “The Chemical Reduction of Poly(tetrafluoroethy1ene) ,” Macromolecules, 21(1988), 3011-3014 27. Christine A. Costello, Thomas J. McCarthy, “ Surface Modification of Poly(tetrafluoroethylene) with Benzoin Dianion,” Macromolecules, 17(1984), 2940-2942 28. Hiroshi Sakurai, Yoshihiro Kubo, Masaru Shiotani, Hidenori Yahiro, Yasuhiro Okuda, “Reduction of Poly(tetrafluoroethylene) by Aromatic RadicalAnions: An ESR and NMR Study,” J. appl. polym. sci., 74(1999), 286-289 29. A. M. Dessouki, N. H. Taher, M. B. El-Arnaouty, “Gamma Ray Induced Graft Copolymerization of N-Vinylpyrrolidone, Acrylamide and Their Mixtures Onto Polypropylene Films,” Polymer International, 45 (1998), 67-76 30. El-Sayed A. Hegazy, N. H. Taher, H. Kamal, “Cationic Membranes From PTFE-g-PMAA,” J. appl. polym. sci., 38(1989), 1229-1242 31. D. J. Wilson, R. L. Williams, R. C. Pond, “Plasma modification of PTFE surfaces,” Surf. Interface Anal., 31(2001), 385-396 32. V. SVORCIK, I. MICEK, V. RYBKA, L. PALMETSHOFER, V. HNATOWICZ, “Ion Beam Ablation of Polytetrafluoroethylene,” J. appl. polym. sci., 69(1999), 1257 - 1261 33. J. Heitz, V. S vorcık, L. Bacakova, K. Rockova, E. Ratajova, T. Gumpenberger, D. Bauerle, B. Dvorankova, H. Kahr, I. Graz, C. Romanin, “Cell adhesion on polytetrafluoroethylene modified by UV-irradiation in an ammonia atmosphere,” J. biomed. materi. res., 67(2003), 130-137 34. SUNG R. KIM, “Surface Modification of Poly(tetrafluoroethylene) Film by Chemical Etching, Plasma, and Ion Beam Treatments,” J. appl. polym. sci., 77(2000), 1913-1920 35. Masashi Miwa, Akira Nakajima, Akira Fujishima, Kazuhito Hashimoto, Toshiya Watanabe, “Effects of the surface roughness on sliding angles of water droplets on superhydrophobic surface,” Langmuir 16(2000), 5754-5760 36. John P. LaFemina, “Surface analytical techniques for probing biomaterial processes,” Edited by John Davies et al., CRC Press, Inc. Boca Raton, USA, (1996) 37. Donald L. Pavia, Gary M. Lampman, George S. Kriz, “Introduction to spectroscopy,” Harcourt, Inc. ,Orlando, (2001) 38. Chittur, k. k., “FTIR/ATR for protein adsorption to biomaterial surfaces,” Biomaterials, 19(1998), 357-369 39. Hari Singh Nalwa, “Advances In Surface Science,” Academic press., London, (2001) 40. Santosh. R. D’Mello, Cinzia. Galli, Teresa. Ciotti, Pietro. Calissano, “Induction of apotosis in cerebellar granule neurons by low potassium: Inhibition of death by insulin-like growth factor I and CAMP,” Proc. Natl. Acad. Sci. 90(1993), 10989-10993 41. Oliver C. Wells, “Scanning electron microscopy,” McGraw-Hill, Inc., USA 42. 黑田行昭原著,上野洋一郎, 溫秋明, 柯俊良, 陳怡菁, 郭順宇, 郭榮烈, 陳泓志, 胡威文, 張傳偉編譯 “組織培養的技術” , 藝軒圖書出版社,台北縣, 台灣, (2002) 43. L. Kavan, J. Kastner, “Carbyne forms carbon：continuation of the story, ”Carbon, 32(1994), 1533-1536 44. J.Kastner, H.Kuzmany, L.Kavan, F.P.Dousek, J.Kurti, “Reductive preparation of carbine with high yield. An raman scattering study, ”Macromolecules, 28(1995), 344-353; zh-TW; http://ntur.lib.ntu.edu.tw/handle/246246/62878; http://ntur.lib.ntu.edu.tw/bitstream/246246/62878/1/ntu-94-R92549023-1.pdf
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16
المؤلفون: 金志龍, Chih-Lung Chin
المساهمون: 劉行讓, Prof. Hsing-Jang Liu
مصطلحات موضوعية: 多重烯環化反應, 還原烷化反應, Diels-Alder反應, 雙萜類天然物, polyene cyclization, reductive-alkylation, Diels-Alder reaction, Diterpenoids
Time: 31
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17
المؤلفون: 葉永城, Young-Cheng Yeh
المساهمون: 王素蘭, Sue-Lein Wang
مصطلحات موضوعية: 層狀鈣矽酸鹽, 水熱合成, 矽烷化反應, layered calcium silicates, hydrothermal, silylation
Time: 31
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Relation: (1)LeBorn, P. C.; Wang, Z.; Pinnavaia, T. J. Applied Clay Science. 1999, 15, 11. (2)Gleiter, H. Adv. Mater. 1992, 4. 474. (3)Komarneni, S. J. Mater. Chem. 1992, 2, 1219. (4)Eckert, H.; Ward. M. Chem. Mater. 2001, 13, 3059. (5)Sanchez, C.; Ribot, F. New J. Chem. 1994, 18, 1007. (6)Novak, B. M. Adv. Mater. 1993, 5, 422. (7)Giannelis, E. P. Adv. Mater. 1996, 8, 29. (8)Okada, A.; Usuki, A. Mater. Sci. Eng. 1995, C3, 109 (9)蔡宗燕，化工資訊，1998，2月刊。 (10)Okada, A.; Kawasumi, M.; Kurauchi, T.; Kamigaito, O. Polym Prepr. 1987, 28, 447. (11)Loy, D. A.; Shea. K. J. Chem. Rev. 1995, 95, 1431. (12)Shea, K. J.; Loy, D. A. Chem. Mater. 2001, 3, 3306. (13)Liu, N.; Yu, K.; Smarsly, B.; Dunphy, D. R.; Jiang, Y. -B.; Brinker, C. J. J. Am. Chem. Soc. 2002, 14, 14540. (14)Lentz, C. W. Inorg. Chem. 1964, 3, 574. (15)Frazier, S. E.; Bedford, J. A.; Hower, J.; Kenny, M. E. Inorg. Chem. 1967, 6, 1693. (16)Ruiz-Hitzky, E.; Rojo, J. M. Nature. 1980, 287, 28. (17)Hefter. J.; Kenny. M. E. J. Am. Chem. Soc. 1981, 103, 5929. (18)Ruiz-Hitzky, E.; Rojo, J. M.; Lagaly, G. Colloid. Polym. Sci. 1985, 263, 1025. (19)Chao, T. C.; Katsoulis, D. E.; Kenny, M. E. Chem. Mater. 2001, 3, 4269 and reference therein. (20)http://content.edu.tw/junior/earth/td_jb/content/s_03/stone/content/stones/sm23.htm (21)Yeh, L. T. Ph. D. Thesis, Case Western Reserve University, Cleveland, Ohio, USA, 1991. (22)林志光, “聚苯乙烯╱蒙脫土奈米複合材料之合成與性質研究”, 私立中原大學論文(2002). (23)Wang, Z.; Lan, T.; Pinnavaia, T. J. Chem. Mater. 1996, 8, 2200. (24)Gies, H.; Marler, B.; Vortmann, S.; Oberhagemann, U.; Bayat, P.; Krink, K.; Rius, J.; Wolf, I.; Fyfe, C. Microporous Mesoporous Mater. 1998, 21, 183. (25)Vortmann, S.; Rius, J.; Marler, B.; Gies, H. Eur. J. Mineral. 1999, 11, 125. (26)Schwieger, W.; Heidemann, D.; Bergk, K. H. Rev. Chim. Minér. 1985, 12, 639. (27)Leu, C.; Wu, Z. W.; Wei, K. H. Chem. Mater. 2002, 14, 3016. (28)Okutomo, S.; Kuroda, K.; Ogawa, M. Applied Clay Science. 1999, 15, 253. (29)Eugster, H. P. Science. 1967, 157, 1177. (30)Rojo, J. M.; Ruiz-Hitzky, E. Sanz. J. Inorg. Chem. 1988, 27, 2785. (31)Okutomo, S.; Kuroda, K.; Ogawa, M. J. Am. Chem. Soc. 1998, 120, 7361. (32)Anderson, T. Phil. Mag. 1851, 1, 111. (33)Mackay, A. L.; Taylor, H. F. W. Mineral. Mag. 1953, 30, 80. (34)http://www.johnbetts-fineminerals.com/. Photo Copyright © 2000-2001 by John H. Betts. All Rights Reserved. (35)Merlino, S. Mineral. Mag. 1988, 52, 377. (36)Chalmers, R. A.; Farmer, V. C.; Harker, R. I.; Kelly, S.; Taylor, H. F.W. Mineral. Mag. 1964, 33, 821. (37)Merlino, S. Mineral. Mag. 1988, 52, 247. (38)Lippmaa, E.; Magi, M.; Samoson, A.; Engelhardt, G.; Grimmer, A. R. J. Am. Chem. Soc. 1980, 102, 4889. (39)Miyake, M.; Iwaya, M.; Suzuki, T. J. Am. Ceram. Soc. 1990, 73(11), 3524. (40)http://www.iupac.org/goldbook/D01751.pdf (41)Okada, Y.; Fang, Y.; Ishida, H.; Nishido, H. Journal of the Ceramic Society of Japan. 1994, 102(May), 452. (42)Buckle, E. R. Journ. Phys. Chem. 1959, 63, 1231. (43)Shimojima, A.; Mochizuki, D.; Kuroda, K. Chem. Mater. 2001, 13, 3603. (44)Gregg, S. J.; Sing, K. S. W. Adsorption, Surface Area and Porosity. Academic Press: London, 1982. (45)Kruk, M.; Jaroniec, M. Chem. Mater. 2001, 13, 3169. (46)Streitwieser, Jr. A.; Heathcock, C. H. Introduction to Organic Chemistry. Macmillan: New York, 18981; (a) p 147-148, (b) p 229, (c) p 278, (d) p 726. (47)http://140.114.18.41/micro/chap11/ch11-2-2.html. (48)Taylor, H. F. W. The Calcium Silicate Hydrates. And reference therein. (49)Meyer, J. W.; Jaunarajs, K. L. Amer. Min. 1961, 43, 913.; http://nthur.lib.nthu.edu.tw/dspace/handle/987654321/27071
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المؤلفون: 陳阿煌, Arh-Hwang Chen
المساهمون: 國立高雄師範大學化學系(所)
Time: 1, 2
وصف الملف: 351 bytes; text/html
Relation: 行政院國家科學委員會計畫 / 計畫編號 NSC93-2113-M017-002; http://ir.nknu.edu.tw/ir//handle/987654321/2354; http://ir.nknu.edu.tw/ir/bitstream/987654321/2354/1/index.html
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19Academic Journal
المساهمون: 北京大学, 内蒙古大学, 北京大学 呼和浩特
المصدر: 知网
Relation: 燃料化学学报.1986,(04),289-296.; 804741; http://hdl.handle.net/20.500.11897/300661
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المؤلفون: 楊德芳
المساهمون: 應用化學系(所)
مصطلحات موضوعية: 醛醇反應, 醛醇, 不對稱合成, 甲醯異冰片, 立體選擇性, 烷化反應, Aldol reaction, Aldol, Asymmetric synthesis, Formyl isoborneol, Stereoselectivity, Alkylation
وصف الملف: application/pdf; 79874 bytes
Relation: http://ir.lib.cyut.edu.tw:8080/handle/310901800/5001; http://ir.lib.cyut.edu.tw:8080/bitstream/310901800/5001/1/樟腦分子醛醇衍生物的不對稱醛醇縮合反應及其產物的烷基化反應.pdf
الاتاحة: http://ir.lib.cyut.edu.tw:8080/handle/310901800/5001
http://ir.lib.cyut.edu.tw:8080/bitstream/310901800/5001/1/樟腦分子醛醇衍生物的不對稱醛醇縮合反應及其產物的烷基化反應.pdf