{"currentpage":1,"firstResult":0,"maxresult":10,"pagecode":5,"pageindex":{"endPagecode":5,"startPagecode":1},"records":[{"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":"合成了3个含硅四烃基二锡氧烷化合物,并通过乙酸与异戊醇的反应和丁醛与乙二醇的反应,考察了它们在酯化反应和缩醛化反应中的催化活性,讨论了催化剂用量、反应时间和溶剂等因素对催化反应的影响.结果表明,与二氯代四丁基二锡氧烷相比,3种含硅四烃基二锡氧烷在酯化反应和缩醛化反应中均表现出类似的高催化活性;催化剂[ClBu2SnOSn(CH2SiMe3)2Cl]2用量为反应物料质量的1.5%时,乙酸异戊酯的产率为91.8%,丁醛缩乙二醇的产率为94.2%.在四烃基二锡氧烷结构中,锡原子上的烃基或桥联基团的不同,对其催化活性均有一定程度的影响.","authors":[{"authorName":"何小立","id":"3d428ee3-95e5-45d1-bb18-8d128128557e","originalAuthorName":"何小立"},{"authorName":"林森","id":"087cac7e-99a0-4930-af7e-3b30053d8d44","originalAuthorName":"林森"},{"authorName":"郭璇","id":"fe47fbf3-4c1a-4e44-a107-313e890b25cd","originalAuthorName":"郭璇"},{"authorName":"陆路德","id":"9cec6b86-10a1-425e-ab65-79abc84c418f","originalAuthorName":"陆路德"},{"authorName":"汪信","id":"bd8905a3-55bb-4397-95ad-bcd87df28394","originalAuthorName":"汪信"},{"authorName":"杨绪杰","id":"cfda73b7-676f-455a-8a9a-9e24e9ce1470","originalAuthorName":"杨绪杰"}],"doi":"10.3969/j.issn.1000-0518.2007.11.010","fpage":"1268","id":"ec8720aa-85a2-4b58-820a-8fae5ba70001","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":"f02d2d5f-09f0-4b2d-ba78-e94e92cf02a9","keyword":"含硅四烃基二锡氧烷","originalKeyword":"含硅四烃基二锡氧烷"},{"id":"0644d0d9-16db-4c24-95e0-bada7f460794","keyword":"合成","originalKeyword":"合成"},{"id":"8bb83849-6fd3-494c-b124-1ef40c4a5197","keyword":"催化","originalKeyword":"催化"},{"id":"4f6ea8a3-6afe-4a38-a3c5-c96860e98fce","keyword":"酯化反应","originalKeyword":"酯化反应"},{"id":"ab9962c0-3d3e-4e74-849f-1d7bff92d2be","keyword":"缩醛化反应","originalKeyword":"缩醛化反应"}],"language":"zh","publisherId":"yyhx200711010","title":"含硅四烃基二锡氧烷的合成及其催化性能","volume":"24","year":"2007"},{"abstractinfo":"以四丁基二锡氧烷为催化剂,通过尿素的醇解反应,合成了四种高沸点碳酸二酯化合物.研究结果表明,尿素的第一步醇解反应较易进行,产物收率大于60%;第二步从氨基甲酸酯醇解变为碳酸二酯的反应较难进行.尿素醇解反应与所用的醇有密切的关系,其中尿素与苯甲醇醇解为碳酸二酯的反应最易进行,正己醇次之,而正辛醇反应最难进行. 提高反应温度到195 ℃,以官能团为NCS的四丁基二锡氧烷代替官能团为Cl的四丁基二锡氧烷为催化剂时,适当提高醇的配比,尿素与正辛醇醇解为碳酸二酯的产物收率有较大的提高. 提出了尿素醇解反应的可能机理.","authors":[{"authorName":"兰支利","id":"4d1ac5f5-7c94-4344-b4d1-15513e6edf54","originalAuthorName":"兰支利"},{"authorName":"吕妍","id":"b5bb708c-71a8-4a2a-8a1d-d48bfcf6374d","originalAuthorName":"吕妍"},{"authorName":"李靖","id":"3cbdd153-20ec-4838-a94e-b301893969e8","originalAuthorName":"李靖"},{"authorName":"谢庆兰","id":"a67708e9-faa2-4360-86c2-99e85c9677cc","originalAuthorName":"谢庆兰"}],"doi":"","fpage":"77","id":"e58461a1-3cc8-4c4b-82f4-ca33a1df343c","issue":"1","journal":{"abbrevTitle":"CHXB","coverImgSrc":"journal/img/cover/CHXB.jpg","id":"18","issnPpub":"0253-9837","publisherId":"CHXB","title":"催化学报 "},"keywords":[{"id":"0bb05d61-d274-4eb5-b388-eaaedd1e6633","keyword":"四丁基二锡氧烷","originalKeyword":"四丁基二锡氧烷"},{"id":"591eb2c1-b00d-4640-8497-cc2023ce0488","keyword":"尿素","originalKeyword":"尿素"},{"id":"9ad666a2-7a0f-4651-8a29-0d4fcba12e82","keyword":"碳酸二酯","originalKeyword":"碳酸二酯"},{"id":"2d43d64b-e16e-42e5-9cb0-bc3dcdf30cc1","keyword":"氨基甲酸酯","originalKeyword":"氨基甲酸酯"}],"language":"zh","publisherId":"cuihuaxb200201018","title":"四丁基二锡氧烷催化合成碳酸二酯类化合物的新方法","volume":"23","year":"2002"},{"abstractinfo":"合成了13种三烃基锡二茂铁甲酸酯类化合物,对化合物进行了元素分析和谱学表征. 化合物生物活性测定表明,其生物选择性主要取决于锡原子上的3个烃基,其中含有环己基、丁基、甲基和RMe2SiCH2基的衍生物具有较好的杀螨活性,而三丁基锡二茂铁甲酸酯的杀菌活性较好.","authors":[{"authorName":"罗宁","id":"23497959-227a-4d2f-98ea-d409b0bc8601","originalAuthorName":"罗宁"},{"authorName":"孙丽娟","id":"19bf1d03-b9c1-424d-a0c4-62684a9d2d5e","originalAuthorName":"孙丽娟"},{"authorName":"刘治中","id":"c334835a-8293-4b35-bb8d-b5b934739500","originalAuthorName":"刘治中"},{"authorName":"谢庆兰","id":"7e001d31-dbf1-451f-bbcb-cc230556b83c","originalAuthorName":"谢庆兰"},{"authorName":"母昭德","id":"dbb26f57-e249-4d9c-b4c8-2bd00038f8e0","originalAuthorName":"母昭德"}],"doi":"10.3969/j.issn.1000-0518.2000.02.010","fpage":"154","id":"c82c8b1f-9a2d-44a1-ae64-def8743544cf","issue":"2","journal":{"abbrevTitle":"YYHX","coverImgSrc":"journal/img/cover/YYHX.jpg","id":"73","issnPpub":"1000-0518","publisherId":"YYHX","title":"应用化学"},"keywords":[{"id":"6f4cd8a0-2af1-4a02-8741-11fd8a69f4a9","keyword":"三烃基锡","originalKeyword":"三烃基锡"},{"id":"df0b4559-c7de-4fa3-9622-d1a674be4144","keyword":"二茂铁甲酸","originalKeyword":"二茂铁甲酸"},{"id":"e337f33d-3de1-4d59-9983-ccce3ed8b9a6","keyword":"谱学表征","originalKeyword":"谱学表征"},{"id":"fb178b15-b2fe-4dfa-9e81-0ff71715307e","keyword":"生物活性","originalKeyword":"生物活性"}],"language":"zh","publisherId":"yyhx200002010","title":"三烃基锡二茂铁甲酸酯的合成、表征及其生物活性","volume":"17","year":"2000"},{"abstractinfo":"以八甲基环四硅氧烷(D4)为主链剂,四甲基二乙烯基二硅氧烷(MM)为封端剂,用碱催化平衡法合成乙烯基聚二甲基硅氧烷(V-PDMS),探讨了影响合成反应及产物分子量、乙烯基含量(Vi%)的主要因素,并对合成的V-PDMS进行精制处理.","authors":[{"authorName":"胡友慧","id":"065075a0-31d6-4d43-8656-831e0f45b834","originalAuthorName":"胡友慧"},{"authorName":"许新社","id":"8e4f5665-f8a0-4bce-81c4-afd7e51f661f","originalAuthorName":"许新社"}],"doi":"","fpage":"67","id":"fcd5cc8d-d74b-4a6a-915b-fc06931a0c85","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":"4a5fd6ea-14db-47f3-b7a3-62c00f2280c8","keyword":"四甲基二乙烯基二硅氧烷","originalKeyword":"四甲基二乙烯基二硅氧烷"},{"id":"9cdb9cf2-f4d0-406f-bd98-1af50ce67992","keyword":"八甲基环四硅氧烷","originalKeyword":"八甲基环四硅氧烷"},{"id":"7dab883f-6436-41e7-a444-4a1ad89ee297","keyword":"聚硅氧烷","originalKeyword":"聚硅氧烷"},{"id":"3e1b9587-f22e-443c-b0ac-14ed184616ac","keyword":"纯化","originalKeyword":"纯化"}],"language":"zh","publisherId":"gfzclkxygc200003019","title":"乙烯基聚二甲基硅氧烷的合成与纯化","volume":"16","year":"2000"},{"abstractinfo":"考察了10种含硅二烃基锡化合物对柠檬醛与乙二醇及环己酮与乙二醇的缩合反应的催化活性.研究了催化剂用量、反应时间、醛醇及酮醇的物质的量之比和溶剂等对反应产率的影响.结果表明,除一种催化剂外,9种化合物对缩醛和缩酮反应均有良好的催化活性,当催化剂用量为反应物质量分数的1.4%,醛与乙二醇的物质量之比为1:1.3,酮与乙二醇的物质量之比为1:1.6,以环己烷为带水剂,回流反应3h,产物收率分别达92%和86%以上.","authors":[{"authorName":"林森","id":"5b8f4a56-d986-41ba-9a4b-d8bacb1bffcb","originalAuthorName":"林森"},{"authorName":"郭杨洋","id":"8a751fb8-904a-4397-9dd6-4e13f565bd2e","originalAuthorName":"郭杨洋"},{"authorName":"邓瑞红","id":"e4f82ee6-407d-4586-a199-ef90404e4ff1","originalAuthorName":"邓瑞红"},{"authorName":"黄志强","id":"5e099e75-3508-40d2-ba7c-3fda3522cb69","originalAuthorName":"黄志强"}],"doi":"10.3724/SP.J.1095.2013.20211","fpage":"271","id":"fde341d4-d292-4803-baa7-23189720e719","issue":"3","journal":{"abbrevTitle":"YYHX","coverImgSrc":"journal/img/cover/YYHX.jpg","id":"73","issnPpub":"1000-0518","publisherId":"YYHX","title":"应用化学"},"keywords":[{"id":"bf429546-c4a9-491d-a056-bcbff57749ea","keyword":"含硅二烃基锡化合物","originalKeyword":"含硅二烃基锡化合物"},{"id":"619cd2bb-1f9f-4425-ae41-edc93443b593","keyword":"催化活性","originalKeyword":"催化活性"},{"id":"82904501-0c68-4d88-8122-5fbd6e984b27","keyword":"缩醛反应","originalKeyword":"缩醛反应"},{"id":"d1e9fec0-5672-40d1-be0f-e1517b6acd16","keyword":"缩酮反应","originalKeyword":"缩酮反应"}],"language":"zh","publisherId":"yyhx201303005","title":"含硅二烃基锡化合物对醇醛(酮)缩合反应的催化活性","volume":"30","year":"2013"},{"abstractinfo":"采用一步法以二甲基二氯硅烷、四氢呋喃和金属镁粉为原料,在碘乙烷和单质碘催化下合成二-(4-羟基丁基)四甲基二硅氧烷.产物温合物减压过滤,以除去镁盐.滤液无需蒸馏提纯,而直接水解,干燥,减压蒸馏,收集71℃/1333Pa馏份.还探讨和优化合成条件:四氢呋喃与二甲基二氯硅烷之摩尔比应大于3.5;Grignard反应停止后应继续加热回流1小时;蒸馏时系统压力为1333Pa.","authors":[{"authorName":"游革新","id":"18b3e304-3a30-4f1a-ad74-4fea584adcb6","originalAuthorName":"游革新"},{"authorName":"赵耀明","id":"f0f53e1e-2a4e-4679-8a73-401ef23e464c","originalAuthorName":"赵耀明"},{"authorName":"刘海敏","id":"d86775a5-42c4-4648-ab7f-bd7a7134535c","originalAuthorName":"刘海敏"},{"authorName":"严玉蓉","id":"f1c0de76-b33a-4322-bcc9-28cde699c620","originalAuthorName":"严玉蓉"},{"authorName":"谭锡荣","id":"bcb8b6ba-eb9f-46a3-b51f-416c797eacee","originalAuthorName":"谭锡荣"}],"doi":"10.3969/j.issn.1671-5381.2003.03.003","fpage":"6","id":"918330b6-78f0-4a89-8d26-1b68a0ec766d","issue":"3","journal":{"abbrevTitle":"HCCLLHYYY","coverImgSrc":"journal/img/cover/HCCLLHYYY.jpg","id":"42","issnPpub":"1671-5381","publisherId":"HCCLLHYYY","title":"合成材料老化与应用"},"keywords":[{"id":"54481ade-7dc7-4917-902f-e0ae474db126","keyword":"硅氧烷","originalKeyword":"硅氧烷"},{"id":"7fdd0f68-ac0f-409d-8b16-b3c449d0edb2","keyword":"二-(4-羟基丁基)四甲基二硅氧烷","originalKeyword":"二-(4-羟基丁基)四甲基二硅氧烷"}],"language":"zh","publisherId":"hccllhyyy200303003","title":"二-(4-羟基丁基)四甲基二硅氧烷的合成研究","volume":"32","year":"2003"},{"abstractinfo":"三苯基氯化锡和烯(或炔)基膦酸二钠反应,合成了8种新的双(三苯基锡)不饱和烃基膦酸酯.利用元素分析、红外光谱、核磁共振氢谱和锡谱以及质谱表征了这些化合物的结构.生物活性测试表明,该类化合物具有很高的杀菌活性.","authors":[{"authorName":"尹汉东","id":"051d8029-7e6c-4e9c-ac3e-2959aaf4b8d8","originalAuthorName":"尹汉东"},{"authorName":"张如芬","id":"c5eb45c6-90c8-4f80-8a94-603e9a78eea2","originalAuthorName":"张如芬"},{"authorName":"马春林","id":"32ce6414-8caf-40ec-8edc-e4a90cf516e6","originalAuthorName":"马春林"}],"doi":"10.3969/j.issn.1000-0518.2001.02.013","fpage":"134","id":"630e4b5a-a6a7-4960-baa1-9708c4b04d32","issue":"2","journal":{"abbrevTitle":"YYHX","coverImgSrc":"journal/img/cover/YYHX.jpg","id":"73","issnPpub":"1000-0518","publisherId":"YYHX","title":"应用化学"},"keywords":[{"id":"acade526-ab67-4549-a882-ea07d27f1adc","keyword":"三苯基锡","originalKeyword":"三苯基锡"},{"id":"77f5e66e-85d4-4ef5-a588-106b9cbda452","keyword":"不饱和烃基膦酸酯.合成","originalKeyword":"不饱和烃基膦酸酯.合成"},{"id":"7171c1cd-37e2-4154-b0ab-95c41c83a174","keyword":"生物活性","originalKeyword":"生物活性"}],"language":"zh","publisherId":"yyhx200102013","title":"双(三苯基锡)不饱和烃基膦酸酯的合成和性质","volume":"18","year":"2001"},{"abstractinfo":"利用双[三(硅烃基亚甲基)锡]氧化物与吡啶甲酸反应,合成了9种三(硅烃基亚甲基)锡吡啶甲酸酯.通过IR、1H NMR、13C NMR、MS以及元素分析测试技术,对这些化合物的结构进行了表征.生物活性的初步测定结果表明,三[(三甲硅基)亚甲基]锡吡啶甲酸酯和三[(乙基二甲基硅基)亚甲基]锡吡啶甲酸酯具有较好的杀螨活性,而三[(丁基二甲基硅基)亚甲基]锡吡啶甲酸酯的杀螨活性较差.","authors":[{"authorName":"林森","id":"8abbd8d4-afd7-48ce-8cca-c2cdf0cb4e3c","originalAuthorName":"林森"},{"authorName":"邓瑞红","id":"c8912be2-c87e-4224-9e1a-1a282b966de1","originalAuthorName":"邓瑞红"},{"authorName":"姚华","id":"cecf1649-689c-436d-a17e-b2168f4a3077","originalAuthorName":"姚华"},{"authorName":"孙小强","id":"a34cc47b-e3e7-4220-847c-5da1cd4766e4","originalAuthorName":"孙小强"},{"authorName":"汪信","id":"eff808c3-2812-4c66-9dad-e7c7cf5359ab","originalAuthorName":"汪信"}],"doi":"10.3969/j.issn.1000-0518.2005.09.015","fpage":"989","id":"1cb46c99-4e56-4d20-a867-958387148cdf","issue":"9","journal":{"abbrevTitle":"YYHX","coverImgSrc":"journal/img/cover/YYHX.jpg","id":"73","issnPpub":"1000-0518","publisherId":"YYHX","title":"应用化学"},"keywords":[{"id":"8ea6de5f-fe57-4034-a194-9647ed012da1","keyword":"含硅有机锡化合物","originalKeyword":"含硅有机锡化合物"},{"id":"dbeb0927-6805-48d5-9bfc-4e37e5f03cc0","keyword":"合成","originalKeyword":"合成"},{"id":"753a3ee0-7236-4d3f-be7d-f24d95af8fc5","keyword":"结构表征","originalKeyword":"结构表征"},{"id":"3f0a5595-897a-4bc2-b0f2-95ebe070271e","keyword":"生物活性","originalKeyword":"生物活性"}],"language":"zh","publisherId":"yyhx200509015","title":"三(三烃硅基亚甲基)锡吡啶甲酸酯的合成和结构表征","volume":"22","year":"2005"},{"abstractinfo":"采用气相色谱内标法,对二-(4-羟基丁基)四甲基二硅氧烷合成产物进行定量分析,并确定了色谱操作条件和产物的重量校正因子.该方法操作简单、快速、精度高、重现性好.","authors":[{"authorName":"游革新","id":"df142f9f-f74d-4811-917f-93616e292ffb","originalAuthorName":"游革新"},{"authorName":"赵耀明","id":"fff04c24-5e70-4fbf-9780-22aa9bf36689","originalAuthorName":"赵耀明"},{"authorName":"严玉蓉","id":"8fcb54e8-f86d-4234-9132-3fe595701c9f","originalAuthorName":"严玉蓉"},{"authorName":"汪朝阳","id":"e60062af-1869-4b4e-8449-106aa1aa4801","originalAuthorName":"汪朝阳"}],"doi":"10.3969/j.issn.1671-5381.2003.02.008","fpage":"21","id":"a8763fc6-aaec-452c-aba9-c3e0d2d074fe","issue":"2","journal":{"abbrevTitle":"HCCLLHYYY","coverImgSrc":"journal/img/cover/HCCLLHYYY.jpg","id":"42","issnPpub":"1671-5381","publisherId":"HCCLLHYYY","title":"合成材料老化与应用"},"keywords":[{"id":"b565efa3-b0dd-4bb5-a0f8-c07837eda151","keyword":"气相色谱","originalKeyword":"气相色谱"},{"id":"f259f757-e0ee-4792-944e-4e6f5ca4b75a","keyword":"内标法","originalKeyword":"内标法"},{"id":"cf5a8180-b9c4-4ae9-a761-9091744b2b9d","keyword":"二-(4-羟基丁基)四甲基二硅氧烷","originalKeyword":"二-(4-羟基丁基)四甲基二硅氧烷"}],"language":"zh","publisherId":"hccllhyyy200302008","title":"气相色谱法测定二-(4-羟基丁基)四甲基二硅氧烷的合成产物含量","volume":"32","year":"2003"}],"totalpage":5902,"totalrecord":59019}