M. Machida, Hirotaka Murakami, Takeshi Kitsubayashi, T. Kijima
{"title":"Erratum: Intercalation of nitric oxide into double-layered cuprate superstructure (Journal of the Chemical Society, Chemical Communications (1995) (485))","authors":"M. Machida, Hirotaka Murakami, Takeshi Kitsubayashi, T. Kijima","doi":"10.1039/C39950001309","DOIUrl":"https://doi.org/10.1039/C39950001309","url":null,"abstract":"","PeriodicalId":17282,"journal":{"name":"Journal of The Chemical Society, Chemical Communications","volume":"9 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"1995-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78626584","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Naphthoquinone methide dyes show a large Pockels coefficient at 1.3 µm when poled in a polymer matrix: the second-order nonlinear hyperpolarizability (µβ) values obtained from Pockels coefficients that appear after poling in a constant electric field are (5700–7400)× 10–48 esu, being much higher than that of commonly used Disperse Red 1 (DR1).
{"title":"Novel naphthoquinone methide dyes for second-order nonlinear optical materials","authors":"Y. Kubo, S. Aramaki, Okamoto Yuko, T. Murayama","doi":"10.1039/C39950000969","DOIUrl":"https://doi.org/10.1039/C39950000969","url":null,"abstract":"Naphthoquinone methide dyes show a large Pockels coefficient at 1.3 µm when poled in a polymer matrix: the second-order nonlinear hyperpolarizability (µβ) values obtained from Pockels coefficients that appear after poling in a constant electric field are (5700–7400)× 10–48 esu, being much higher than that of commonly used Disperse Red 1 (DR1).","PeriodicalId":17282,"journal":{"name":"Journal of The Chemical Society, Chemical Communications","volume":"124 1","pages":"969-970"},"PeriodicalIF":0.0,"publicationDate":"1995-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86902660","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
T. Oshikawa,, M. Yamashita,, Sadaaki Kumagai, K. Seo, J. Kobayashi
Various amines and alcohols are converted into the corresponding phosphamides by the action of optically active diazacyclophosphamidic chlorides and absolute configurations of amines and alcohols are readily determined by proton and phosphorus NMR of the cyclophosphamides that are formed.
{"title":"Optically active diazacyclophosphamides: novel efficient reagents for the determination of the absolute configuration of amines and alcohols","authors":"T. Oshikawa,, M. Yamashita,, Sadaaki Kumagai, K. Seo, J. Kobayashi","doi":"10.1039/C39950000435","DOIUrl":"https://doi.org/10.1039/C39950000435","url":null,"abstract":"Various amines and alcohols are converted into the corresponding phosphamides by the action of optically active diazacyclophosphamidic chlorides and absolute configurations of amines and alcohols are readily determined by proton and phosphorus NMR of the cyclophosphamides that are formed.","PeriodicalId":17282,"journal":{"name":"Journal of The Chemical Society, Chemical Communications","volume":"49 1","pages":"435-436"},"PeriodicalIF":0.0,"publicationDate":"1995-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75330667","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Transmetallation of 4- and 5-benzyloxypent-2-enyl(tributyl)stannanes 13 and 18 with tin(IV) chloride generates intermediate allyltin trichlorides which react with imines 9 and ent-9, prepared from butyl glyoxylate and either (R)- or (S)-1-phenylethylamine, with effective 1,5-asymmetric induction.
{"title":"Remote asymmetric induction in reactions between 4- and 5-benzyloxypent-2-enyl(tributyl)stannanes and chiral imines prepared from butyl glyoxylate","authors":"D. Hallett, E. Thomas","doi":"10.1039/C39950000657","DOIUrl":"https://doi.org/10.1039/C39950000657","url":null,"abstract":"Transmetallation of 4- and 5-benzyloxypent-2-enyl(tributyl)stannanes 13 and 18 with tin(IV) chloride generates intermediate allyltin trichlorides which react with imines 9 and ent-9, prepared from butyl glyoxylate and either (R)- or (S)-1-phenylethylamine, with effective 1,5-asymmetric induction.","PeriodicalId":17282,"journal":{"name":"Journal of The Chemical Society, Chemical Communications","volume":"12 1","pages":"657-658"},"PeriodicalIF":0.0,"publicationDate":"1995-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91185479","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The enantiomeric purity of aromatic substrates can be determined using 31P NMR with chiral rhodium complexes in situ.
芳香底物的对映体纯度可以用手性铑配合物原位31P NMR测定。
{"title":"A SIMPLE IN SITU 31P NMR METHOD FOR THE DETERMINATION OF THE ENANTIOMERIC PURITY OF AROMATIC SUBSTRATES","authors":"J. Buriak, J. Osborn","doi":"10.1039/C39950000689","DOIUrl":"https://doi.org/10.1039/C39950000689","url":null,"abstract":"The enantiomeric purity of aromatic substrates can be determined using 31P NMR with chiral rhodium complexes in situ.","PeriodicalId":17282,"journal":{"name":"Journal of The Chemical Society, Chemical Communications","volume":"121 10 1","pages":"689-690"},"PeriodicalIF":0.0,"publicationDate":"1995-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84090097","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A new telogen for telechelic oligomers of chlorotrifluoroethylene","authors":"R. Chambers, M. Greenhall, A. Wright, G. Caporiccio","doi":"10.1039/C39910001323","DOIUrl":"https://doi.org/10.1039/C39910001323","url":null,"abstract":"A new telogen, I(CF2CFCl)nl (n= 1) and its telomers (n= average 6) are obtained by irradiation of mixtures of iodine and Chlorotrifluoroethylene.","PeriodicalId":17282,"journal":{"name":"Journal of The Chemical Society, Chemical Communications","volume":"29 1","pages":"1323-1324"},"PeriodicalIF":0.0,"publicationDate":"1995-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78798308","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Powder X-ray diffraction, 29Si and 129Xe NMR spectroscopy of MCM-41 show that the long-range structural order and textural uniformity of the mesoporous molecular sieve are markedly improved due to a shift in the reaction equilibrium when acetic acid is repeatedly added during the conversion of sodium silicate and NMe3(C16H33)Cl to a MCM-41 phase.
{"title":"Structural order in MCM-41 controlled by shifting silicate polymerization equilibrium","authors":"R. Ryoo, Ji Man Kim","doi":"10.1039/C39950000711","DOIUrl":"https://doi.org/10.1039/C39950000711","url":null,"abstract":"Powder X-ray diffraction, 29Si and 129Xe NMR spectroscopy of MCM-41 show that the long-range structural order and textural uniformity of the mesoporous molecular sieve are markedly improved due to a shift in the reaction equilibrium when acetic acid is repeatedly added during the conversion of sodium silicate and NMe3(C16H33)Cl to a MCM-41 phase.","PeriodicalId":17282,"journal":{"name":"Journal of The Chemical Society, Chemical Communications","volume":"148 1","pages":"711-712"},"PeriodicalIF":0.0,"publicationDate":"1995-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76623204","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The use of a tandem Ireland Claisen rearrangement followed by an in situ silicon mediated epoxide fragmentation provides an efficient entry into 1,3-dienes containing an E-double bond and an exo-methylene group; initial results regarding remote chirality control are reported.
{"title":"The construction of 1,3-dienes containing an E-double bond and an exo-methylene group","authors":"J. Eshelby, P. Parsons, N. C. Sillars, P. Crowley","doi":"10.1039/C39950001497","DOIUrl":"https://doi.org/10.1039/C39950001497","url":null,"abstract":"The use of a tandem Ireland Claisen rearrangement followed by an in situ silicon mediated epoxide fragmentation provides an efficient entry into 1,3-dienes containing an E-double bond and an exo-methylene group; initial results regarding remote chirality control are reported.","PeriodicalId":17282,"journal":{"name":"Journal of The Chemical Society, Chemical Communications","volume":"20 1","pages":"1497-1498"},"PeriodicalIF":0.0,"publicationDate":"1995-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73662484","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Iodination of 5,15-diphenylporphyrin followed by metallation and palladium(0) catalysed coupling with monosubstituted acetylenes gives zinc(II)-10-(2-substituted-alkynyl)-5,15-diphenylporphyrins.
{"title":"Iodination and Heck alkynylation of 5,15-diphenylporphyrin. A convenient entry to asymmetrically meso-substituted porphyrins","authors":"R. Boyle, Claire K. Johnson, D. Dolphin","doi":"10.1039/C39950000527","DOIUrl":"https://doi.org/10.1039/C39950000527","url":null,"abstract":"Iodination of 5,15-diphenylporphyrin followed by metallation and palladium(0) catalysed coupling with monosubstituted acetylenes gives zinc(II)-10-(2-substituted-alkynyl)-5,15-diphenylporphyrins.","PeriodicalId":17282,"journal":{"name":"Journal of The Chemical Society, Chemical Communications","volume":"31 1","pages":"527-528"},"PeriodicalIF":0.0,"publicationDate":"1995-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73793733","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
V. Vidal, A. Théolier, J. Thivolle-cazat, J. Basset
Silica-supported tantalum hydride activates at low temperature the C–H and the C–D bonds of cyclooctane and CD4, respectively, to form the corresponding cyclooctyl and perdeuteriomethyl-tantalum surface complexes; these complexes are transformed under molecular oxygen into the corresponding tantalum-alkoxy derivatives which with acetic acid give rise to the corresponding alkylacetates.
{"title":"Activation and functionalisation of the C–H bonds of methane and higher alkanes by a silica-supported tantalum hydride complex","authors":"V. Vidal, A. Théolier, J. Thivolle-cazat, J. Basset","doi":"10.1039/C39950000991","DOIUrl":"https://doi.org/10.1039/C39950000991","url":null,"abstract":"Silica-supported tantalum hydride activates at low temperature the C–H and the C–D bonds of cyclooctane and CD4, respectively, to form the corresponding cyclooctyl and perdeuteriomethyl-tantalum surface complexes; these complexes are transformed under molecular oxygen into the corresponding tantalum-alkoxy derivatives which with acetic acid give rise to the corresponding alkylacetates.","PeriodicalId":17282,"journal":{"name":"Journal of The Chemical Society, Chemical Communications","volume":"6 1","pages":"991-992"},"PeriodicalIF":0.0,"publicationDate":"1995-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74002108","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
京公网安备 11010802042870号
京ICP备2023020795号-1
扫码关注我们
求助内容：
应助结果提醒方式：