稀有金属材料与工程, 2006, 35(z1): 438-441.
高温气体净化用金属多孔材料的发展现状
张健 1, , 汤慧萍 2, , 奚正平 3, , 汪强兵 {"currentpage":1,"firstResult":0,"maxresult":10,"pagecode":5,"pageindex":{"endPagecode":5,"startPagecode":1},"records":[{"abstractinfo":"首次使用固相法制备出了分子内电荷移动型(CT type)共轭聚合物聚(3,6-二噻基.哒嗪)(P(DThPD)),在25℃测得聚合物的特性黏度为0.67 dL/g.并利用核磁共振谱(1H-NMR)、红外光谱(FT-IR)、紫外.可见光谱(UV-vis)、电子扫描显微镜(SEM)、电子透射显微镜(TEM)、元素分析(elemental analysis)、循环伏安(CV)等测试方法对聚合物进行了表征.结果表明,DThPD在研磨过程中在d,d'位置发生了聚合反应,生成了纳米粒子聚合物,并且聚合物具有一定的电化学活性.","authors":[{"authorName":"张子印","id":"b52638c9-5072-451f-a81e-bf75319f0b83","originalAuthorName":"张子印"},{"authorName":"刘彩霞","id":"ee603dc6-fe6f-4753-8dfb-b9915fd7a581","originalAuthorName":"刘彩霞"},{"authorName":"宋微娜","id":"f49992c3-3a42-4f43-b0ce-bcede672de9c","originalAuthorName":"宋微娜"},{"authorName":"殷德刚","id":"4aa16027-7479-4fbb-9173-376a8b0b92b1","originalAuthorName":"殷德刚"},{"authorName":"司马义·努尔拉","id":"32081c6f-c8ab-4b65-8f97-462a1a40ea93","originalAuthorName":"司马义·努尔拉"}],"doi":"","fpage":"28","id":"e2a54d34-7fb0-4971-8115-a256ac674d2c","issue":"3","journal":{"abbrevTitle":"GFZCLKXYGC","coverImgSrc":"journal/img/cover/GFZCLKXYGC.jpg","id":"31","issnPpub":"1000-7555","publisherId":"GFZCLKXYGC","title":"高分子材料科学与工程"},"keywords":[{"id":"9525ec24-bdda-4146-91e8-5f80b81f1fe8","keyword":"固相聚合","originalKeyword":"固相聚合"},{"id":"175eb470-e86f-4f6d-902a-f96128b7f083","keyword":"聚(3,6-二噻基-哒嗪)","originalKeyword":"聚(3,6-二噻基-哒嗪)"},{"id":"90895224-bdf6-4274-aadd-1db02f131aad","keyword":"共轭聚合物","originalKeyword":"共轭聚合物"},{"id":"feb18637-49a8-43a1-a76b-2c05956cf521","keyword":"Pd(PPh3)4催化剂","originalKeyword":"Pd(PPh3)4催化剂"}],"language":"zh","publisherId":"gfzclkxygc200903008","title":"分子内电荷移动型共轭聚合物的固相法制备及表征","volume":"25","year":"2009"},{"abstractinfo":"由3,6-二氯哒嗪和脂肪醇在(C4H9)4NBr作相转移催化剂和浓碱存在下,合成了3-氯-6-烷氧基哒嗪.后者在三苯基膦钯的催化下,与对胆甾氧羰基苯基硼酸偶联,合成了8种中心桥连基为哒嗪环,含有苯环,胆甾基,酯基,不同烷氧基长度的3-烷氧基-6-(4-胆甾氧羰基苯基)哒嗪.用DSC法对其介晶性进行了表征,发现其中7种都具有介晶性.研究结果还表明,末端链长度对相变温度和清亮点温度均有影响,但对介晶相温度范围影响较小.","authors":[{"authorName":"熊俊如","id":"7adb5bd5-2644-4c5a-b1c6-707da58d6722","originalAuthorName":"熊俊如"},{"authorName":"向清祥","id":"18759e06-88d5-4e17-b823-cb93b35b27fd","originalAuthorName":"向清祥"},{"authorName":"张元勤","id":"20dd6710-d3f7-4a5d-8e13-cae1d1eb6533","originalAuthorName":"张元勤"}],"doi":"10.3969/j.issn.1000-0518.2003.11.016","fpage":"1088","id":"d8940f5b-7b4c-4c45-b003-79681ec137c1","issue":"11","journal":{"abbrevTitle":"YYHX","coverImgSrc":"journal/img/cover/YYHX.jpg","id":"73","issnPpub":"1000-0518","publisherId":"YYHX","title":"应用化学"},"keywords":[{"id":"b0323598-d05c-4302-a2d1-edd213263cb2","keyword":"哒嗪衍生物","originalKeyword":"哒嗪衍生物"},{"id":"78b5a818-6394-4d53-9a85-dc5056cdc92a","keyword":"合成","originalKeyword":"合成"},{"id":"b389dec2-c575-4855-b577-fae792bcd06e","keyword":"介晶性","originalKeyword":"介晶性"}],"language":"zh","publisherId":"yyhx200311016","title":"3,6-双取代哒嗪的合成和介晶性","volume":"20","year":"2003"},{"abstractinfo":"报道了一种新型三组分反应策略用于区域选择性合成一系列三取代的哒嗪,即于水中进行DABCO催化的苯丙酮、芳香乙二醛一水合物和水合肼三组分缩合反应。该法提供了一种绿色便利的一锅法制备各种芳基取代的3,6-二芳基-4-甲基哒嗪,它以水为溶剂, DABCO为绿色碱有机催化剂,具有高区域选择性、操作简便、产物收率高和后处理简单等优点。","authors":[{"authorName":"Mehdi Rimaz","id":"55522a61-30fa-43a6-956a-4663c53c5e09","originalAuthorName":"Mehdi Rimaz"},{"authorName":"Farkhondeh Aali","id":"3b3776f5-2643-46ed-aad5-7b3faf6115d0","originalAuthorName":"Farkhondeh Aali"}],"doi":"10.1016/S1872-2067(15)61060-9|","fpage":"517","id":"ca2dd741-106a-45eb-835b-e01ec3120891","issue":"4","journal":{"abbrevTitle":"CHXB","coverImgSrc":"journal/img/cover/CHXB.jpg","id":"18","issnPpub":"0253-9837","publisherId":"CHXB","title":"催化学报 "},"keywords":[{"id":"eaaad42a-c667-44fe-a468-31c3575f47f2","keyword":"1,4-二氮杂二环2.2.2辛烷","originalKeyword":"1,4-二氮杂二环2.2.2辛烷"},{"id":"220914f0-bfa6-47c3-a711-f7362a34de92","keyword":"苯丙酮","originalKeyword":"苯丙酮"},{"id":"e17dd3a5-a820-4c9b-a727-e350d1f07b54","keyword":"芳香乙二醛一水合物","originalKeyword":"芳香乙二醛一水合物"},{"id":"a7ddda3f-0044-4f0b-b964-0824c70e937b","keyword":"哒嗪","originalKeyword":"哒嗪"}],"language":"zh","publisherId":"cuihuaxb201604008","title":"环境友好碱有机催化一锅法区域选择性合成新型3,6-二芳基-4-甲基哒嗪","volume":"37","year":"2016"},{"abstractinfo":"以四(三苯基磷)钯(Pd(PPh3)4)和CuI作为催化剂,在二异丙胺和四氢呋喃溶液中,采用宽能带的1,4-二乙炔基-2,5-二(十二烷氧基)苯(PE)和窄能带的3,6-双(5′-溴-2′-噻吩)-哒嗪(TPD)以不同配料比合成了一系列新型聚芳炔.长链烷氧基的存在使得此类聚合物在常用的有机溶剂中具有较好的溶解性和成膜性.通过对上述聚合物的紫外-可见吸收、荧光发射及循环伏安等基本性能进行探讨可知,共聚物在THF溶液中的荧光量子效率为51%～61%;随着共聚物中TPD含量的增加,共聚物薄膜的吸收起始波长及荧光发射波长均有红移.聚合物薄膜的最大发射峰位于540～551nm.","authors":[{"authorName":"秦红梅","id":"bdc31c52-39ac-4ee1-b790-2525303aff0d","originalAuthorName":"秦红梅"},{"authorName":"石伟","id":"00357341-3686-4d93-b59b-2833b2b8f210","originalAuthorName":"石伟"},{"authorName":"茹克亚木·买提斯迪克","id":"e495dfbf-d55c-432f-a1c6-516dca3c86fd","originalAuthorName":"茹克亚木·买提斯迪克"},{"authorName":"韩燕","id":"0a1f4236-8777-49ec-8aab-4c40cea83eba","originalAuthorName":"韩燕"},{"authorName":"黎万丽","id":"a9e1af2b-f9b2-41e7-895a-5c54f2ae46ce","originalAuthorName":"黎万丽"},{"authorName":"司马义·努尔拉","id":"f30f5134-703b-4145-b335-78296e472b26","originalAuthorName":"司马义·努尔拉"}],"doi":"","fpage":"1406","id":"a31ea8e5-112f-44a3-b4f3-31c45123ee5c","issue":"8","journal":{"abbrevTitle":"GNCL","coverImgSrc":"journal/img/cover/GNCL.jpg","id":"33","issnPpub":"1001-9731","publisherId":"GNCL","title":"功能材料"},"keywords":[{"id":"34765405-cdb2-4c3b-add7-8d3799ac5cef","keyword":"聚芳炔","originalKeyword":"聚芳炔"},{"id":"b62760b3-9376-4cdc-969c-60d85bdf3155","keyword":"哒嗪","originalKeyword":"哒嗪"},{"id":"98097803-9798-4fd9-bae8-3d3548b95496","keyword":"噻吩","originalKeyword":"噻吩"}],"language":"zh","publisherId":"gncl201008030","title":"含二噻基哒嗪的聚芳炔类衍生物的合成与性能研究","volume":"41","year":"2010"},{"abstractinfo":"采用改进的方法,以NaH作为碱,在温和条件下通过二氢奎尼丁和3,6-二氯哒嗪的亲核取代反应合成了手性配体3,6-双(9-O-二氢奎尼丁)哒嗪((DHQD)2PYDZ), 配体的产率为78%. 以N-氯代氨基甲酸苄酯钠为氧化-供氮试剂,由(DHQD)2PYDZ与OsO4原位生成的催化剂在6种烯烃的不对称氨羟化反应中表现出较高的立体选择性(83%～92%)和区域选择性(79:21～88:12),反应主产物的化学产率为40%～76%.","authors":[{"authorName":"程司堃","id":"b58580d8-b489-4383-a8f5-a726e1759c40","originalAuthorName":"程司堃"},{"authorName":"张生勇","id":"3f40c8f7-ab29-4f07-8ad3-2642ef602355","originalAuthorName":"张生勇"},{"authorName":"李晓晔","id":"561e19ee-d00c-408b-8ba6-ef8dd1aab242","originalAuthorName":"李晓晔"},{"authorName":"姜茹","id":"e7a1c4a1-c7c6-454e-8b09-b4a466236ae4","originalAuthorName":"姜茹"},{"authorName":"南鹏娟","id":"8c913665-4b0d-4c77-899a-a048ec0d2b84","originalAuthorName":"南鹏娟"}],"doi":"","fpage":"621","id":"b0cd9953-3ad1-47d3-a88a-29fa0f86336a","issue":"7","journal":{"abbrevTitle":"CHXB","coverImgSrc":"journal/img/cover/CHXB.jpg","id":"18","issnPpub":"0253-9837","publisherId":"CHXB","title":"催化学报 "},"keywords":[{"id":"903d7060-6e5c-4eeb-9d34-674ec786f6c8","keyword":"手性配体","originalKeyword":"手性配体"},{"id":"6e740e19-7c64-4e44-9041-e633ff90577b","keyword":"3,6-双(9-O-二氢奎尼丁)哒嗪","originalKeyword":"3,6-双(9-O-二氢奎尼丁)哒嗪"},{"id":"0ccf8da1-51bb-4c0b-9d45-d9cff8bbe442","keyword":"烯烃","originalKeyword":"烯烃"},{"id":"68f6e283-6067-4744-bfc6-f87b6d4900c9","keyword":"不对称氨羟化","originalKeyword":"不对称氨羟化"},{"id":"c60669da-e0b9-4b2b-9de4-c10edf221eb0","keyword":"手性β-氨基醇","originalKeyword":"手性β-氨基醇"}],"language":"zh","publisherId":"cuihuaxb200507020","title":"手性配体3,6-双(9-O-二氢奎尼丁)哒嗪的合成及其在烯烃不对称氨羟化反应中的催化性能","volume":"26","year":"2005"},{"abstractinfo":"以苯、丁二酸酐为原料,经傅克酰基化,硝化,与水合肼反应三步反应合成6-(3-氨基苯基)-4,5-二氢哒嗪-3(2H)-酮(1),总收率为58.3％.由3-(3-硝基苯甲酰基)丙酸(3)合成化合物1的过程中,在雷尼镍(Raney Ni)的催化下与水合肼反应,一步完成了苯环上硝基的还原和成环.重点考察了该步反应的物料配比、反应时间对产率的影响.结果表明,水合肼与化合物3的摩尔比11.7∶1,回流反应4h,产率为82.7％.","authors":[{"authorName":"江刘平","id":"89630ccc-6bc6-440c-ab8e-8f52edeba194","originalAuthorName":"江刘平"},{"authorName":"康从民","id":"fd11c55f-c7cc-4ea7-a421-609663ec433c","originalAuthorName":"康从民"},{"authorName":"吕英涛","id":"6d0622bd-4e12-4fe4-a76d-66962858b3da","originalAuthorName":"吕英涛"}],"doi":"10.3724/SP.J.1095.2014.30635","fpage":"1191","id":"cb8030c9-9b04-45da-b109-82639c9acad3","issue":"10","journal":{"abbrevTitle":"YYHX","coverImgSrc":"journal/img/cover/YYHX.jpg","id":"73","issnPpub":"1000-0518","publisherId":"YYHX","title":"应用化学"},"keywords":[{"id":"463559b9-156c-445c-9122-3547ff8558c4","keyword":"(氨基苯基)-二氢哒嗪-3 (2H)-酮","originalKeyword":"(氨基苯基)-二氢哒嗪-3 (2H)-酮"},{"id":"ce6e00b6-77c7-41e9-bbc0-e9fbad1ffce3","keyword":"雷尼镍","originalKeyword":"雷尼镍"},{"id":"94a2001c-93f0-4de9-b69e-7a6a27c92c1a","keyword":"水合肼","originalKeyword":"水合肼"}],"language":"zh","publisherId":"yyhx201410011","title":"6-(3-氨基苯基)4,5-二氢哒嗪-3(2H)-酮的合成","volume":"31","year":"2014"},{"abstractinfo":"由6-羟基-2-苯基-3-哒嗪酮和二丁基氧化锡合成了新的有机锡氧簇化合物Ⅰ,用元素分析、IR、1H、13C和119Sn NMR表征了其结构.由X射线单晶衍射测定了其晶体结构,该化合物属于三斜晶系,P1空间群,晶体学参数为a=1.221 75(13)nm,b=1.267 90(13)nm,c=1.345 33(14)nm,α=87.168 0(10)°,β=672.265 0(10)°,γ=87.261 0(10)°,V=1.981 4(4)nm3,Z=1,Dc=1.435 g/cm3,μ(MoKα)=0.870 0,F(000)=868.该化合物具有中心对称的梯形结构,锡原子为五配位的三角双锥构型.该化合物催化乙酰乙酸乙酯和甲醇的酯交换的产率为88%、催化丙二酸二甲酯和乙醇的酯交换的产率为90%,但较难催化环己酮和甘油的缩酮反应,产率低于22%.","authors":[{"authorName":"毛武涛","id":"04665c7c-f8df-4da3-aca4-735db517c1cb","originalAuthorName":"毛武涛"},{"authorName":"田来进","id":"2d8b8e2b-1d83-43ac-b008-9b5985484eec","originalAuthorName":"田来进"},{"authorName":"郑晓风","id":"225ab9f3-fa42-4d15-8956-aedf3aebf846","originalAuthorName":"郑晓风"},{"authorName":"尹玲","id":"7ab86bce-8dfc-482b-baa9-7802d1f76cde","originalAuthorName":"尹玲"}],"doi":"10.3969/j.issn.1000-0518.2007.12.005","fpage":"1368","id":"e214903e-260d-4e82-a63b-1b2793902f77","issue":"12","journal":{"abbrevTitle":"YYHX","coverImgSrc":"journal/img/cover/YYHX.jpg","id":"73","issnPpub":"1000-0518","publisherId":"YYHX","title":"应用化学"},"keywords":[{"id":"4b175dd2-c346-4d21-b1af-85303fd73582","keyword":"四烃基二锡氧烷","originalKeyword":"四烃基二锡氧烷"},{"id":"e8af8a74-4cab-4c4c-961c-7e184a5aa5e0","keyword":"羟基苯基哒嗪酮","originalKeyword":"羟基苯基哒嗪酮"},{"id":"a062bd30-958e-41dd-883b-192b80438610","keyword":"催化活性","originalKeyword":"催化活性"},{"id":"32be49d9-c971-4312-a689-7c7172c95868","keyword":"晶体结构","originalKeyword":"晶体结构"}],"language":"zh","publisherId":"yyhx200712005","title":"6-羟基-2-苯基-3-哒嗪酮四丁基二锡氧烷二聚体的合成、表征和催化性能","volume":"24","year":"2007"},{"abstractinfo":"在相转移催化条件下,2,3,4,6-四-O-乙酰基-1-溴-1-脱氧-α-D-吡喃葡萄糖1与6-(4-卤代苯基)-3(2H)-哒嗪酮2反应,合成了4种新的哒嗪酮葡萄糖苷3;然后用干燥的氨气在0～-5 ℃下处理,得相应的2-N-(β-D-吡喃葡萄糖-1-基)-6-(4-卤代苯基)-3-哒嗪酮4. 这些化合物的结构经IR、1H NMR、13C NMR及元素分析所证实.","authors":[{"authorName":"辛炳炜","id":"e0a9f119-5f40-4703-b482-3e9f40a55504","originalAuthorName":"辛炳炜"},{"authorName":"孙昌俊","id":"531b3654-7ccc-4db9-9454-723fd8ec7c38","originalAuthorName":"孙昌俊"},{"authorName":"曲立强","id":"aef16c12-ed79-4be2-b33b-777790207156","originalAuthorName":"曲立强"},{"authorName":"曹晓冉","id":"52db1667-1bad-4b6f-a8df-720ca640add0","originalAuthorName":"曹晓冉"}],"doi":"10.3969/j.issn.1000-0518.2003.06.019","fpage":"590","id":"18cfd13f-9d34-448d-8ba1-915bc94db223","issue":"6","journal":{"abbrevTitle":"YYHX","coverImgSrc":"journal/img/cover/YYHX.jpg","id":"73","issnPpub":"1000-0518","publisherId":"YYHX","title":"应用化学"},"keywords":[{"id":"19ed904d-7f7f-4f17-8c86-8fcba55741e7","keyword":"哒嗪酮葡萄糖苷","originalKeyword":"哒嗪酮葡萄糖苷"},{"id":"ec9362f1-8fd8-45a1-ba95-6f81f0276f98","keyword":"合成,相转移催化","originalKeyword":"合成,相转移催化"}],"language":"zh","publisherId":"yyhx200306019","title":"糖苷合成研究(ⅩⅩⅠ)2-N-(β-D-吡喃葡萄糖-1-基)-6-(4-卤代苯基)-3-哒嗪酮的合成","volume":"20","year":"2003"},{"abstractinfo":"以二价钯配合物作为催化剂,将2-异丙基氨基-4,6-二(2'-溴-3,4-乙撑二氧噻基)-1,3,5-三嗪分别与1,4-二乙炔基-2,5-二辛氧基苯、1,4-二乙炔基-2,5-二(十二烷氧基)苯、2,7-二(4,4,5,5-四甲基硼烷基)-9,9-二辛基芴交替共聚合成了3种π-共轭聚合物P1,P2和P3.经傅里叶变换红外光谱、氢核磁共振谱、紫外-可见光谱、荧光光谱、循环伏安法、X射线粉末衍射和凝胶渗透色谱等测试手段对其进行了表征,并对聚合物在CHCl3溶液的酸致变色行为进行了研究.结果表明,得到的聚合物在CHCl3中的紫外-可见最大吸收波长分别在443 nm和431 nm处出现.在CHCl3溶液中聚合物P1,P2和P3最大发射峰分别位于507 nm,511 nm和543 nm,其聚合物薄膜的最大发射波长分别为573 nm,557 nm和559nm.与P1和P2相比,P3的酸致变色敏感性高于2个数量级.聚合物P1和P2均在-2.0～0 V出现n-掺杂峰.聚合物X射线衍射谱图显示聚合物均有一定的结晶性.","authors":[{"authorName":"阿布都克尤木·阿布都热西提","id":"2f669227-f0e3-44a9-b4f9-43af5070ea6a","originalAuthorName":"阿布都克尤木·阿布都热西提"},{"authorName":"阿卜杜合拜尔·米尔扎","id":"d1c0b810-590a-4669-ae03-0e679795663a","originalAuthorName":"阿卜杜合拜尔·米尔扎"},{"authorName":"古丽加娜提·排他尔","id":"3f1eef28-993d-4e0c-b236-e2613e7df944","originalAuthorName":"古丽加娜提·排他尔"},{"authorName":"拜合提亚·艾海提","id":"bd7466b3-4151-4d5e-ab9c-e72388951bbe","originalAuthorName":"拜合提亚·艾海提"},{"authorName":"吐尼莎古丽·阿吾提","id":"387cbd8a-2118-407b-a78d-2b07baf3be37","originalAuthorName":"吐尼莎古丽·阿吾提"},{"authorName":"司马义·努尔拉","id":"a79c0339-ad40-4385-84e1-c436c8d3777f","originalAuthorName":"司马义·努尔拉"}],"doi":"","fpage":"34","id":"fe711d60-b691-4e8b-b5f9-1ab495d09ab9","issue":"6","journal":{"abbrevTitle":"GFZCLKXYGC","coverImgSrc":"journal/img/cover/GFZCLKXYGC.jpg","id":"31","issnPpub":"1000-7555","publisherId":"GFZCLKXYGC","title":"高分子材料科学与工程"},"keywords":[{"id":"2a9ed840-4fb5-410d-95ac-c965dc007059","keyword":"2-异丙基氨基-4,6-二(2'-溴-3,4-乙撑二氧噻基)-1,3,5-三嗪","originalKeyword":"2-异丙基氨基-4,6-二(2'-溴-3,4-乙撑二氧噻基)-1,3,5-三嗪"},{"id":"102fe6ca-74da-4a3b-af7f-ef5113167ce1","keyword":"π-共轭聚合物","originalKeyword":"π-共轭聚合物"},{"id":"ba6dbbb5-fd2e-4c75-a99f-98593065bf78","keyword":"酸致变色","originalKeyword":"酸致变色"},{"id":"27cf6373-4682-47e2-b373-a56a8d0273c7","keyword":"二价钯配合物","originalKeyword":"二价钯配合物"}],"language":"zh","publisherId":"gfzclkxygc201506007","title":"含2-异丙基氨基-4,6-二(3,4-乙撑二氧噻基)-1,3,5-三嗪π-共轭聚合物的合成及性能","volume":"31","year":"2015"},{"abstractinfo":"合成了1-取代苯基-1,4-二氢-6-甲基-4-哒嗪酮-3-酰肼化合物. 生物活性测定表明,该类化合物对烟草花叶病毒具有很高的抑制作用,并且对水稻纹枯病具有优良的抑制作用.","authors":[{"authorName":"邹霞娟","id":"e3f49be4-ba8f-41b6-85e9-19e55744ed0b","originalAuthorName":"邹霞娟"},{"authorName":"金桂玉","id":"ebfb3840-fedc-40cf-a8d4-ee70b3a3e0c9","originalAuthorName":"金桂玉"},{"authorName":"杨昭","id":"76f0ffd8-b9bd-45e4-a474-93af4a3e63ca","originalAuthorName":"杨昭"}],"doi":"10.3969/j.issn.1000-0518.2001.08.002","fpage":"599","id":"4155a319-3cd2-4d53-aac8-2254f4d539b9","issue":"8","journal":{"abbrevTitle":"YYHX","coverImgSrc":"journal/img/cover/YYHX.jpg","id":"73","issnPpub":"1000-0518","publisherId":"YYHX","title":"应用化学"},"keywords":[{"id":"674f8b3c-6100-48de-b74c-93d1d3173e1f","keyword":"哒嗪酮","originalKeyword":"哒嗪酮"},{"id":"062708b1-4958-42f8-b274-fa8e6ebcbf7a","keyword":"合成","originalKeyword":"合成"},{"id":"fc275414-1c73-4cf4-9a7e-6873f2b2a5a2","keyword":"植物病毒抑制活性","originalKeyword":"植物病毒抑制活性"}],"language":"zh","publisherId":"yyhx200108002","title":"1-取代苯基-1,4-二氢-6-甲基-4-哒嗪酮-3-酰肼的合成及其抗烟草花叶病毒活性","volume":"18","year":"2001"}],"totalpage":9622,"totalrecord":96217}