H. Krueger, Nicole M. Shapiro, E. Bosch, D. Unruh, R. Groeneman
{"title":"二次相互作用对含等构给体的卤素键共晶结构多样性的影响","authors":"H. Krueger, Nicole M. Shapiro, E. Bosch, D. Unruh, R. Groeneman","doi":"10.3390/compounds2040023","DOIUrl":null,"url":null,"abstract":"The formation of a pair of co-crystals based upon isosteric halogen-bond donors, namely 1,4-diiodoperchlorobenzene and iodoperchlorobenzene, along with the acceptor 4,4-bipyridine is reported. As expected, the components in each co-crystal engage in halogen bonding interactions resulting in a one-dimensional chain-like structure. In particular, the co-crystal containing 1,4-diiodoperchlorobenzene is primarily held together by I···N halogen bonds while the solid based upon iodoperchlorobenzene forms both I···N and Cl···N interactions. Structural diversity is achieved between these co-crystals based upon the type of secondary interactions involving the chlorine atoms on each halogen-bond donor even though they are isosteric in nature.","PeriodicalId":10621,"journal":{"name":"Compounds","volume":"104 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Influence of Secondary Interactions on Structural Diversity between a Pair of Halogen-Bonded Co-Crystals Containing Isosteric Donors\",\"authors\":\"H. Krueger, Nicole M. Shapiro, E. Bosch, D. Unruh, R. Groeneman\",\"doi\":\"10.3390/compounds2040023\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The formation of a pair of co-crystals based upon isosteric halogen-bond donors, namely 1,4-diiodoperchlorobenzene and iodoperchlorobenzene, along with the acceptor 4,4-bipyridine is reported. As expected, the components in each co-crystal engage in halogen bonding interactions resulting in a one-dimensional chain-like structure. In particular, the co-crystal containing 1,4-diiodoperchlorobenzene is primarily held together by I···N halogen bonds while the solid based upon iodoperchlorobenzene forms both I···N and Cl···N interactions. Structural diversity is achieved between these co-crystals based upon the type of secondary interactions involving the chlorine atoms on each halogen-bond donor even though they are isosteric in nature.\",\"PeriodicalId\":10621,\"journal\":{\"name\":\"Compounds\",\"volume\":\"104 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-10-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Compounds\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/compounds2040023\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Compounds","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/compounds2040023","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Influence of Secondary Interactions on Structural Diversity between a Pair of Halogen-Bonded Co-Crystals Containing Isosteric Donors
The formation of a pair of co-crystals based upon isosteric halogen-bond donors, namely 1,4-diiodoperchlorobenzene and iodoperchlorobenzene, along with the acceptor 4,4-bipyridine is reported. As expected, the components in each co-crystal engage in halogen bonding interactions resulting in a one-dimensional chain-like structure. In particular, the co-crystal containing 1,4-diiodoperchlorobenzene is primarily held together by I···N halogen bonds while the solid based upon iodoperchlorobenzene forms both I···N and Cl···N interactions. Structural diversity is achieved between these co-crystals based upon the type of secondary interactions involving the chlorine atoms on each halogen-bond donor even though they are isosteric in nature.