Nadia Maté , Elena Bogdan , Lidia Căta , Anamaria Terec , Arie van der Lee , Mihail Bӑrboiu , Niculina D. Hӑdade , Ion Grosu
{"title":"作为多孔超分子材料多功能候选材料的大型多功能三苯胺衍生物","authors":"Nadia Maté , Elena Bogdan , Lidia Căta , Anamaria Terec , Arie van der Lee , Mihail Bӑrboiu , Niculina D. Hӑdade , Ion Grosu","doi":"10.1016/j.tet.2025.134630","DOIUrl":null,"url":null,"abstract":"<div><div>The access to novel triphenyl-, tris(biphenyl)- and tris(phenyl-ethynyl-phenyl)amine derivatives decorated with bromine, carboxy or hydroxymethyl groups is developed based on aliphatic nucleophilic substitution and Suzuki-Miyaura and Sonogashira cross-coupling reactions. The target compounds decorated with various groups are able to participate to the formation of self-assembled architectures by hydrogen or halogen bonding.</div></div>","PeriodicalId":437,"journal":{"name":"Tetrahedron","volume":"178 ","pages":"Article 134630"},"PeriodicalIF":2.1000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Large multifunctional triphenylamine derivatives as versatile candidates for porous supramolecular materials\",\"authors\":\"Nadia Maté , Elena Bogdan , Lidia Căta , Anamaria Terec , Arie van der Lee , Mihail Bӑrboiu , Niculina D. Hӑdade , Ion Grosu\",\"doi\":\"10.1016/j.tet.2025.134630\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The access to novel triphenyl-, tris(biphenyl)- and tris(phenyl-ethynyl-phenyl)amine derivatives decorated with bromine, carboxy or hydroxymethyl groups is developed based on aliphatic nucleophilic substitution and Suzuki-Miyaura and Sonogashira cross-coupling reactions. The target compounds decorated with various groups are able to participate to the formation of self-assembled architectures by hydrogen or halogen bonding.</div></div>\",\"PeriodicalId\":437,\"journal\":{\"name\":\"Tetrahedron\",\"volume\":\"178 \",\"pages\":\"Article 134630\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-03-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0040402025001863\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0040402025001863","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Large multifunctional triphenylamine derivatives as versatile candidates for porous supramolecular materials
The access to novel triphenyl-, tris(biphenyl)- and tris(phenyl-ethynyl-phenyl)amine derivatives decorated with bromine, carboxy or hydroxymethyl groups is developed based on aliphatic nucleophilic substitution and Suzuki-Miyaura and Sonogashira cross-coupling reactions. The target compounds decorated with various groups are able to participate to the formation of self-assembled architectures by hydrogen or halogen bonding.
期刊介绍:
Tetrahedron publishes full accounts of research having outstanding significance in the broad field of organic chemistry and its related disciplines, such as organic materials and bio-organic chemistry.
Regular papers in Tetrahedron are expected to represent detailed accounts of an original study having substantially greater scope and details than that found in a communication, as published in Tetrahedron Letters.
Tetrahedron also publishes thematic collections of papers as special issues and ''Reports'', commissioned in-depth reviews providing a comprehensive overview of a research area.