{"currentpage":1,"firstResult":0,"maxresult":10,"pagecode":5,"pageindex":{"endPagecode":5,"startPagecode":1},"records":[{"abstractinfo":"合成了新的发光分子-4-N,N-二苯基氛基苯甲酸琉角酸亚胺(简称TBA-SCM ),利用其琉拍跳亚胺基与PAMAM所含的氛基之间高度反应活性,将三苯胺甲统基组装键合在树枝分子PAMAM (0～3G)表面,构筑新的树枝分子TBA-PAMAM.研究表明,在稀溶液(10-6)下未观测到TBA-PAMAM的<span style=\"color:red\">荧光</span><span style=\"color:red\">增强</span>现象;当浓度增大至10-4时,按1:1的配比组装数秒后即可检测到显著的<span style=\"color:red\">荧光</span><span style=\"color:red\">增强</span>.光谱测试证实,这是由于该浓度下PAMAM聚集态的发光带与TBA-SCM发光带发生部分重叠促进两者之间有效的电荷转移所致.<span style=\"color:red\">荧光</span>衰减曲线拟合结果表明,TBA-PAMAM(OG,3G)有两个寿命,长寿命对应着PAM-AM(0～3G),寿命则是TBA-PAMAM(OG,3G)树枝状结构.随着TBA-SCM的增大,TBA-PAMAM(OG,3G)的单<span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>急剧降低直至完全淬灭,但<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>强度则显著增高.","authors":[{"authorName":"贾美琳","id":"6d355b26-426c-48af-9329-b37e67db9327","originalAuthorName":"贾美琳"},{"authorName":"王筱梅","id":"28b05439-cdca-47df-9069-c3528c5533d9","originalAuthorName":"王筱梅"},{"authorName":"张唯舟","id":"eac60d06-7d4a-4009-bd3d-3d92e24dd917","originalAuthorName":"张唯舟"},{"authorName":"杨平","id":"6b3950d2-b60c-4797-aa9c-1027ceefb82a","originalAuthorName":"杨平"},{"authorName":"王晓宏","id":"cd4d6ac6-d741-4055-9186-71c370025493","originalAuthorName":"王晓宏"},{"authorName":"罗建芳","id":"dca80d04-a5d8-49fe-947f-9075146cac79","originalAuthorName":"罗建芳"}],"doi":"","fpage":"1137","id":"59d16dc0-29ca-45bb-80f0-5a510f8825a7","issue":"6","journal":{"abbrevTitle":"GNCL","coverImgSrc":"journal/img/cover/GNCL.jpg","id":"33","issnPpub":"1001-9731","publisherId":"GNCL","title":"功能材料"},"keywords":[{"id":"072adcdb-bfcf-4729-aa20-562f3dc277a0","keyword":"TBA-PAMAM树枝分子","originalKeyword":"TBA-PAMAM树枝分子"},{"id":"85d6fcf5-7c5d-476b-ad36-b2248cb6279a","keyword":"TBA-SCM","originalKeyword":"TBA-SCM"},{"id":"ab3e5f91-bd5c-4445-ab62-9c334bd435d7","keyword":"快速<span style=\"color:red\">荧光</span><span style=\"color:red\">增强</span>","originalKeyword":"快速荧光增强"},{"id":"2333d9f0-511d-431b-86e4-b7a066419e65","keyword":"<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span><span style=\"color:red\">增强</span>","originalKeyword":"双光子荧光增强"}],"language":"zh","publisherId":"gncl201106046","title":"三苯胺-PAMAM树枝分子的单／<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span><span style=\"color:red\">增强</span>","volume":"42","year":"2011"},{"abstractinfo":"在合成的一类三元离子缔合型铕配合物Eu(tta)4·DEASP中,阳离子基团DEASP做为Eu3+的<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>敏化剂,将Eua+的<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>激发波长拓展至生物光学窗口的长波波段1.06μm.在此基础上合成出一系列DEASP的衍生物,研究阳离子基团的推拉电子能力对于配合物<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>敏化效率的作用机制.通过改变阳离子基团的端基结构可以有效提高<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>敏化效率,有望获得1.06μm高效<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收诱导<span style=\"color:red\">荧光</span>的铕<span style=\"color:red\">荧光</span>探针.","authors":[{"authorName":"史萌","id":"bf2b9547-6f90-41bb-9c70-4a2ca92ff8d8","originalAuthorName":"史萌"},{"authorName":"李华","id":"5b82eb6b-444e-49f5-adf2-c5d70cd6fd41","originalAuthorName":"李华"},{"authorName":"苏富芳","id":"3a5e28a4-76c2-4e41-83f5-62b3a6944b40","originalAuthorName":"苏富芳"},{"authorName":"韩培高","id":"8426f3e9-ed82-4346-bf28-487241782950","originalAuthorName":"韩培高"},{"authorName":"马丽丽","id":"d3001f0f-2ebd-47ab-9227-a9b646bb849e","originalAuthorName":"马丽丽"},{"authorName":"吴福全","id":"f4d10d68-b27c-450d-9a9b-426bfdda4458","originalAuthorName":"吴福全"}],"doi":"10.3969/j.issn.1007-5461.2011.02.009","fpage":"172","id":"8b5bccb3-f75e-47d2-b962-ee613fb66f42","issue":"2","journal":{"abbrevTitle":"LZDZXB","coverImgSrc":"journal/img/cover/LZDZXB.jpg","id":"53","issnPpub":"1007-5461","publisherId":"LZDZXB","title":"量子电子学报   "},"keywords":[{"id":"4d5aa328-4be0-477c-8084-50a9ff05b6f0","keyword":"非线性光学","originalKeyword":"非线性光学"},{"id":"7a83e5db-4852-409f-b24f-9f2932f95bc5","keyword":"铕配合物","originalKeyword":"铕配合物"},{"id":"38e1def8-543b-4233-a028-726eb101a449","keyword":"离子缔合","originalKeyword":"离子缔合"},{"id":"8fb43d0c-51f1-4756-b6d5-7937eddf3f65","keyword":"<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收","originalKeyword":"双光子吸收"}],"language":"zh","publisherId":"lzdzxb201102009","title":"铕配合物<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收诱导<span style=\"color:red\">荧光</span>的研究","volume":"28","year":"2011"},{"abstractinfo":"以具有不同烷基链的2-溴烷基芴和不同末端基团的取代苯乙烯为原料，利用Heck反应合成了五个新型的芴类衍生物(M1~M5)。通过IR、1HNMR和元素分析对目标分子的结构进行了表征，并对它们的紫外吸收，单、<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>光谱进行了测试和分析。结果表明，末端基团的给电子能力越强，紫外和<span style=\"color:red\">荧光</span>光谱的红移程度越大，而且<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收截面也越大；通过改变芴环9位的柔性链长度可以对化合物的溶解性进行调节，但对化合物的光学性能不会产生影响。","authors":[{"authorName":"李道学","id":"c387b9e0-fbd0-48a3-9029-930fc1aed363","originalAuthorName":"李道学"},{"authorName":"冯燕","id":"d11ef127-e144-47a0-864f-f44313938028","originalAuthorName":"冯燕"},{"authorName":"汪俊","id":"a177bd0e-9ad2-4ae3-94a3-286128d25634","originalAuthorName":"汪俊"},{"authorName":"王奇","id":"eb62c8e4-e937-47bd-88ed-a8abccde0926","originalAuthorName":"王奇"},{"authorName":"吕奇","id":"ca832c2d-32ea-46c8-a127-d393c6884c6c","originalAuthorName":"吕奇"},{"authorName":"黄佑红","id":"8437df66-d37e-4784-9f7b-57c17c089305","originalAuthorName":"黄佑红"},{"authorName":"李怡文","id":"5f08cc08-64ec-4910-8062-206681fb0852","originalAuthorName":"李怡文"},{"authorName":"汪新","id":"38dd26e1-bd12-4a6b-98fc-af9423bfc32e","originalAuthorName":"汪新"}],"doi":"10.3969/j.issn.1001-9731.2015.06.011","fpage":"6053","id":"a4871836-048c-4bc6-a52f-ac952d0d3162","issue":"6","journal":{"abbrevTitle":"GNCL","coverImgSrc":"journal/img/cover/GNCL.jpg","id":"33","issnPpub":"1001-9731","publisherId":"GNCL","title":"功能材料"},"keywords":[{"id":"88d4dc61-001a-4d0d-b88e-3a455b4c8a26","keyword":"芴类衍生物","originalKeyword":"芴类衍生物"},{"id":"6f84c1e2-1e65-4655-97cb-7e438b466da2","keyword":"合成","originalKeyword":"合成"},{"id":"b8d81d10-0b48-4f6d-80bd-4ac8b736dd3a","keyword":"给电子能力","originalKeyword":"给电子能力"},{"id":"2c17dd76-d173-485e-9fed-b11347dc68a8","keyword":"单<span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>","originalKeyword":"单光子荧光"},{"id":"3e6b886d-2145-43b7-9954-924607dd8a3e","keyword":"<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>","originalKeyword":"双光子荧光"}],"language":"zh","publisherId":"gncl201506011","title":"具有<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>的芴类衍生物的合成及光学性能?","volume":"","year":"2015"},{"abstractinfo":"以三苯胺基和苯并噻二唑基为电子给、受体,合成得\"D-A-D\"型红光分子(简称TZ2),研究了其在介质中(THF和PVK中)单<span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>(OPL)、<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>(TPL)和电致发光(EL)性能.分别在Xe灯(455nm)和飞秒钛宝石激光器(820nm)泵浦下,TZ2在THF介质中的单<span style=\"color:red\">光子</span>、<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>峰位分别在650和635nm处;在9V电压下,TZ2掺杂在PVK介质中(ITO和FLi/Al分别正、负电极)开始发光,峰位在620nm处.与OPL相比,TPL和EL在发光峰位和光谱半高宽(FWHH)均较为相近,说明激子复合发光(EL)与强光辐照发光(TPL)有更多的相似性.","authors":[{"authorName":"王晓宏","id":"ffe84e33-b3f2-49f5-9845-1e0ac9a174b0","originalAuthorName":"王晓宏"},{"authorName":"王筱梅","id":"68ea5a7e-5ce0-45e9-bb00-68811be3cf3b","originalAuthorName":"王筱梅"},{"authorName":"杨兴淮","id":"55274cdf-b840-42f0-bb6f-9e73a5a11d3c","originalAuthorName":"杨兴淮"},{"authorName":"李瑞","id":"e794cada-51f2-41ad-b1d2-8ecfc24f5624","originalAuthorName":"李瑞"},{"authorName":"罗建芳","id":"b5305387-46e1-477b-99b7-b14489dcbe35","originalAuthorName":"罗建芳"}],"doi":"","fpage":"1211","id":"1d16593e-c872-4396-a360-4b9a90aa653a","issue":"7","journal":{"abbrevTitle":"GNCL","coverImgSrc":"journal/img/cover/GNCL.jpg","id":"33","issnPpub":"1001-9731","publisherId":"GNCL","title":"功能材料"},"keywords":[{"id":"e7db86ad-8d77-4dc5-8a60-1786c6753a25","keyword":"<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>","originalKeyword":"双光子荧光"},{"id":"adde0112-98e3-4fb4-a090-ffa01dae438d","keyword":"有机电致发光","originalKeyword":"有机电致发光"},{"id":"e07f035f-02c4-4f9e-afbe-a369e5730bad","keyword":"三苯胺","originalKeyword":"三苯胺"},{"id":"be715909-677c-478c-a2c4-e1a7f073cfb0","keyword":"苯并噻二唑","originalKeyword":"苯并噻二唑"}],"language":"zh","publisherId":"gncl201007028","title":"苯并噻二唑/三苯胺衍生物合成与<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>、电致发光性能研究","volume":"41","year":"2010"},{"abstractinfo":"用800nm波长的飞秒Ti:sapphire激光测定了2个对称型噁二唑衍生物2,5-二[4-(2-N,N-二苯氨基苯乙烯基)苯基]-1,3,4-噁二唑(PASPO)与2,5-二[4-{2-N,N-二(4-溴代苯)氨基苯乙烯基]苯基}-1,3,4-噁二唑(BrPASPO)的<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收和<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>激发<span style=\"color:red\">荧光</span>光谱,其飞秒<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收截面为20.6和9.91GM,<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>泵浦上转换<span style=\"color:red\">荧光</span>最大波长分别在535和545nm.测定了紫外吸收、<span style=\"color:red\">荧光</span>光谱,研究了化合物在不同溶剂中的溶致变色效应.化合物PASPO和Br-PASPO在二氯甲烷溶液中的吸收峰分别位于412和403nm,<span style=\"color:red\">荧光</span>发射峰分别位于511和495nm,<span style=\"color:red\">荧光</span>量子产率分别为0.73和0.70.","authors":[{"authorName":"钱鹰","id":"1a69ac04-f675-40ba-a9d8-eef9292fb436","originalAuthorName":"钱鹰"},{"authorName":"朱晓勤","id":"f32ebcb3-6d01-4686-b85b-e21eb0b3bb87","originalAuthorName":"朱晓勤"},{"authorName":"黄维","id":"19ce1049-94b6-4066-bd1d-54f75028dea2","originalAuthorName":"黄维"},{"authorName":"吕昌贵","id":"5376d6d6-15a6-4a83-be7c-7ecfed3cf5ff","originalAuthorName":"吕昌贵"},{"authorName":"林国强","id":"07d904db-d504-4ae8-8724-f9b9601957dd","originalAuthorName":"林国强"},{"authorName":"崔一平","id":"bcf1669c-7551-4d3d-9b33-1154aa0c4c98","originalAuthorName":"崔一平"}],"doi":"","fpage":"1774","id":"f6b80d46-085d-4caa-83da-8e33aa275174","issue":"11","journal":{"abbrevTitle":"GNCL","coverImgSrc":"journal/img/cover/GNCL.jpg","id":"33","issnPpub":"1001-9731","publisherId":"GNCL","title":"功能材料"},"keywords":[{"id":"462569d9-078d-48c7-b959-2be4b2aeb45e","keyword":"对称化合物","originalKeyword":"对称化合物"},{"id":"67417594-3535-471f-86c3-b6ea32b6da20","keyword":"<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收","originalKeyword":"双光子吸收"},{"id":"f8531d9c-ef32-475b-b20c-5e17b0cccf79","keyword":"上转换<span style=\"color:red\">荧光</span>","originalKeyword":"上转换荧光"}],"language":"zh","publisherId":"gncl200811003","title":"用飞秒Ti:sapphire激光测定对称型化合物的<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收和上转换<span style=\"color:red\">荧光</span>","volume":"39","year":"2008"},{"abstractinfo":"固相反应合成了新型丙二腈类化合物. 反应0.5 h完成,产率高达93%以上. 采用IR、 UV 、1H NMR及元素分析对产物进行了表征,并通过单晶X射线衍射确定了其中1种化合物的结构. 研究表明,产物具有单<span style=\"color:red\">光子</span>和<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收<span style=\"color:red\">荧光</span>效应,并表现出类似的溶剂效应.","authors":[{"authorName":"马文","id":"087ba3de-6e1a-4122-8082-e6a18f65be0e","originalAuthorName":"马文"},{"authorName":"张胜义","id":"30168303-d5a1-42e1-95eb-b39bf501bad3","originalAuthorName":"张胜义"},{"authorName":"吴杰颖","id":"2e12d04c-f2e6-4b8c-8aa9-e4100d8e5fcf","originalAuthorName":"吴杰颖"},{"authorName":"田玉鹏","id":"d7eec049-8009-4e0c-b8c5-b584a81a90e8","originalAuthorName":"田玉鹏"},{"authorName":"FUN Hoong-Kun","id":"1f40609f-7be3-4564-a1db-af35893e9fd2","originalAuthorName":"FUN Hoong-Kun"}],"doi":"10.3969/j.issn.1000-0518.2003.09.011","fpage":"862","id":"38fcc1f9-c207-4f0b-b1af-5255c7d295c6","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":"e5186f1d-d4ed-4118-bcca-6200a0bd0f0a","keyword":"丙二腈类化合物","originalKeyword":"丙二腈类化合物"},{"id":"26996dd9-7e63-4ae8-a1b5-f67516c9e485","keyword":"室温固相反应","originalKeyword":"室温固相反应"},{"id":"faa42902-3b49-40f4-b20e-46ffc4f3460c","keyword":"<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>","originalKeyword":"双光子荧光"}],"language":"zh","publisherId":"yyhx200309011","title":"丙二腈类化合物的室温固相合成、结构及单<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>性质","volume":"20","year":"2003"},{"abstractinfo":"本工作合成了具有D-π-A-π-D对称结构的化合物2,5-<span style=\"color:red\">双</span>(对二甲氨基苯乙烯基)吡嗪.利用飞秒激光器研究了2,5-<span style=\"color:red\">双</span>(对二甲氨基苯乙烯基)吡嗪的<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收特性,获得了在820nm处的最大<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收截面(σ=212 GM).<span style=\"color:red\">荧光</span>发射强度与激发光强平方的线性关系证明了2,5-<span style=\"color:red\">双</span>(对二甲氨基苯乙烯基)吡嗪的<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>诱导发光机制.","authors":[{"authorName":"郝永超","id":"18f24b33-ccce-419f-9c6a-d5beb28142f5","originalAuthorName":"郝永超"},{"authorName":"陈懿","id":"39e4eb8a-c271-4776-9fff-5c027aec4c53","originalAuthorName":"陈懿"}],"doi":"10.7517/j.issn.1674-0475.2015.04.315","fpage":"315","id":"61ad7c36-e4fb-400e-b4d7-6fccb3b5d211","issue":"4","journal":{"abbrevTitle":"YXKXYGHX","coverImgSrc":"journal/img/cover/YXKXYGHX.jpg","id":"74","issnPpub":"1674-0475","publisherId":"YXKXYGHX","title":"影像科学与光化学   "},"keywords":[{"id":"68bfc39b-9712-4ece-97cd-e2a49e40daa1","keyword":"2,5-<span style=\"color:red\">双</span>(对二甲氨基苯乙烯基)吡嗪","originalKeyword":"2,5-双(对二甲氨基苯乙烯基)吡嗪"},{"id":"272700d1-5835-44ea-986b-14b12fda30ea","keyword":"<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>诱导<span style=\"color:red\">荧光</span>","originalKeyword":"双光子诱导荧光"},{"id":"2bb46a45-d2b0-4ee8-9c36-c61a6d61cf77","keyword":"<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收","originalKeyword":"双光子吸收"},{"id":"327f14f3-c5a5-4c73-83f6-e7b779b6cfee","keyword":"飞秒激光","originalKeyword":"飞秒激光"}],"language":"zh","publisherId":"ggkxyghx201504007","title":"2,5-<span style=\"color:red\">双</span>(对二甲氨基苯乙烯基)吡嗪的<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>诱导<span style=\"color:red\">荧光</span>性质","volume":"33","year":"2015"},{"abstractinfo":"合成了一种新型<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收材料氰基联苯乙烯类化合物,通过元素分析、电喷雾质谱、1H NMR和红外对其进行表征.测试了紫外吸收光谱、单<span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>光谱、单<span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>寿命和<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>光谱.其<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收截面为1.32×10-48cm4·s·photon-1,是潜在应用前景的<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收材料.","authors":[{"authorName":"孙梅","id":"427b159d-acee-46b9-b6c4-885a2a182c04","originalAuthorName":"孙梅"},{"authorName":"胡寒梅","id":"664564e2-a5ec-4625-8361-b590f776d204","originalAuthorName":"胡寒梅"},{"authorName":"田玉鹏","id":"b6ff804a-4a9d-4d0a-a964-d7603b5007b2","originalAuthorName":"田玉鹏"},{"authorName":"蒋民华","id":"273dc53b-4433-4099-8fc5-0801f5aef9a4","originalAuthorName":"蒋民华"}],"doi":"","fpage":"1439","id":"b6b7d408-8497-408e-b5b3-0c6862d9ca38","issue":"9","journal":{"abbrevTitle":"GNCL","coverImgSrc":"journal/img/cover/GNCL.jpg","id":"33","issnPpub":"1001-9731","publisherId":"GNCL","title":"功能材料"},"keywords":[{"id":"4e58c627-524a-4d6f-ad26-d025070adfc6","keyword":"氰基","originalKeyword":"氰基"},{"id":"8943029c-feba-4ada-abfb-5d67de8981d1","keyword":"<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收","originalKeyword":"双光子吸收"},{"id":"340e655c-ea18-4782-a43e-d9c7244ba496","keyword":"<span style=\"color:red\">荧光</span>","originalKeyword":"荧光"}],"language":"zh","publisherId":"gncl200909008","title":"氰基联苯乙烯类<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收材料的合成","volume":"40","year":"2009"},{"abstractinfo":"合成了一种新的有机染料1,2,4,5-四(4-吡啶乙烯基)苯1,2,4,5-tetrakis(4-pyridylvinyl)benzene(简称为:TVPB)并测试了其<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>性质.溶剂缓慢挥发法得到了其反应中间体1,2,4,5-四(二甲氧基膦酰甲基)苯1,2,4,5-tetra (dimethoxyphosphorylmethyl)benzene(简称为:TDMPMB)的晶体.用X射线四圆衍射仪对晶体结构进行了解析.","authors":[{"authorName":"王蕾","id":"49477e0e-bcee-4f36-9ff4-922edf5b1297","originalAuthorName":"王蕾"},{"authorName":"陶绪堂","id":"cbc5e76f-40ee-4453-a1e6-685a2caad6b6","originalAuthorName":"陶绪堂"},{"authorName":"杨家祥","id":"a7df5854-cf6a-4e7d-95d6-0b958e88b9eb","originalAuthorName":"杨家祥"},{"authorName":"于文涛","id":"1877ba18-85f3-42b6-b5b1-36df6bc9fbc3","originalAuthorName":"于文涛"},{"authorName":"任燕","id":"4450ed64-e2d7-4818-90ae-e94765cf956c","originalAuthorName":"任燕"},{"authorName":"辛倩","id":"67a0de00-3b81-4159-8437-e3562b3e8932","originalAuthorName":"辛倩"},{"authorName":"延云兴","id":"46a61c2c-a1fa-4277-ab56-2e6860ba4fe3","originalAuthorName":"延云兴"},{"authorName":"刘陟","id":"1ba93406-f658-405c-a1d1-725caa9f9a1a","originalAuthorName":"刘陟"},{"authorName":"蒋民华","id":"f9c27321-db22-4826-a961-63a0432464bd","originalAuthorName":"蒋民华"}],"doi":"","fpage":"212","id":"b4fd4288-7d39-49d5-8b31-a9350cabcdfa","issue":"z1","journal":{"abbrevTitle":"GNCL","coverImgSrc":"journal/img/cover/GNCL.jpg","id":"33","issnPpub":"1001-9731","publisherId":"GNCL","title":"功能材料"},"keywords":[{"id":"db1796c3-27b4-42dc-9232-9a378a31916b","keyword":"C34H26N4","originalKeyword":"C34H26N4"},{"id":"3a12ae74-7cec-42f4-b056-3097d7631f2c","keyword":"<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收","originalKeyword":"双光子吸收"},{"id":"1f50d1e3-6876-4032-811e-c35f41380069","keyword":"有机染料","originalKeyword":"有机染料"}],"language":"zh","publisherId":"gncl2004z1044","title":"一种有机染料的<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>性质及反应中间体的晶体结构","volume":"35","year":"2004"},{"abstractinfo":"合成了一种具有<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>活性的蓝色发光材料9,10-二咪唑甲基蒽,通过元素分析、电喷雾质谱、1H NMR和红外对其进行表征.测试了紫外吸收光谱、单<span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>光谱、量子产率、单<span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>寿命和<span style=\"color:red\">双</span><span style=\"color:red\">光子</span><span style=\"color:red\">荧光</span>光谱.<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>吸收截面为17×10-50 cm4·s·photon-1,结果表明,是具潜在应用前景的<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>激发蓝光发光材料.","authors":[{"authorName":"孙梅","id":"24ae5fb7-31b1-4b19-a2a4-744b61de5389","originalAuthorName":"孙梅"},{"authorName":"丁大勇","id":"dc735252-bc90-4511-a7c0-51a39808eb1d","originalAuthorName":"丁大勇"},{"authorName":"胡寒梅","id":"22a4e436-ea87-485a-81f8-4d0bcc4a4047","originalAuthorName":"胡寒梅"},{"authorName":"周海鸥","id":"adee7034-dcaf-4088-9519-770654af04c0","originalAuthorName":"周海鸥"},{"authorName":"田玉鹏","id":"89157999-e26c-44c0-a77e-8f9f325103c0","originalAuthorName":"田玉鹏"}],"doi":"10.3969/j.issn.1000-0518.2006.08.026","fpage":"933","id":"67524c0d-74b1-4e92-9532-9854a399ee66","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":"347d745a-3aed-40a9-b169-5c8e2221e7ec","keyword":"<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>","originalKeyword":"双光子"},{"id":"8c53655e-2736-4968-9df3-9fb686355b9b","keyword":"<span style=\"color:red\">荧光</span>","originalKeyword":"荧光"},{"id":"14e64672-7d1f-470c-8a89-f069d3d28d6c","keyword":"蓝色发光材料","originalKeyword":"蓝色发光材料"}],"language":"zh","publisherId":"yyhx200608026","title":"具有<span style=\"color:red\">双</span><span style=\"color:red\">光子</span>活性的蓝色发光材料的合成","volume":"23","year":"2006"}],"totalpage":2227,"totalrecord":22267}