Dr. María Lago-Silva, Manuel Fernández-Míguez, Dr. Zulema Fernández, Prof. María Magdalena Cid, Prof. Emilio Quiñoá, Dr. Rafael Rodríguez, Prof. Félix Freire
{"title":"高阻手性烯超分子聚集体中的共轴螺旋","authors":"Dr. María Lago-Silva, Manuel Fernández-Míguez, Dr. Zulema Fernández, Prof. María Magdalena Cid, Prof. Emilio Quiñoá, Dr. Rafael Rodríguez, Prof. Félix Freire","doi":"10.1002/anie.202421310","DOIUrl":null,"url":null,"abstract":"<p>Chiral allenes self-assembly following a cooperative mechanism into a supramolecular chiral aggregate consisting of two coaxial helices: the internal helix described by the allene stack and the external helix which consist in a 4-helix described by the four allene substituents. More precisely, this supramolecular aggregate possesses six axially chiral elements within its structure—the allene, the allene stack (internal helix) and the stacks of the four allene substituents (external 4-helix)—. Interestingly, slight variations in the magnitude of the tilting degree while keeping its <i>P</i>- or <i>M</i>- orientation (internal helix) can vary the orientation of the 4-axial motifs at the external helix. Thus, while (<i>P</i>)-<b>1</b> produces a supramolecular helix with a Θ ca. 15° (<i>P</i><sub>int</sub>) and a <i>M<sub>1</sub></i>/<i>P<sub>2</sub></i>/<i>M</i><sub><i>1’</i></sub>/<i>P</i><sub><i>2’</i></sub> orientation of the four axial motifs at the periphery, (<i>P</i>)-<b>2</b> produces a supramolecular helix with a Θ ca. 23° (<i>P</i><sub>int</sub>) and a <i>P<sub>1</sub></i>/<i>P<sub>2</sub></i>/<i>P</i><sub><i>1’</i></sub>/<i>P</i><sub><i>2’</i></sub> orientation of the four axial motifs at the external helix. As a result, the ECD spectra and the AFM images of the (<i>P</i>)-<b>1</b> and (<i>P</i>)-<b>2</b> supramolecular aggregates dominated by the 1 and 1’ substituents of the chiral allene indicate opposite handedness although the chirality of the building block and the orientation of the allene stack are the same</p>","PeriodicalId":125,"journal":{"name":"Angewandte Chemie International Edition","volume":"64 10","pages":""},"PeriodicalIF":16.9000,"publicationDate":"2024-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/anie.202421310","citationCount":"0","resultStr":"{\"title\":\"Coaxial Helices in Chiral Supramolecular Aggregates from Highly Hindered Chiral Allenes\",\"authors\":\"Dr. María Lago-Silva, Manuel Fernández-Míguez, Dr. Zulema Fernández, Prof. María Magdalena Cid, Prof. Emilio Quiñoá, Dr. Rafael Rodríguez, Prof. Félix Freire\",\"doi\":\"10.1002/anie.202421310\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Chiral allenes self-assembly following a cooperative mechanism into a supramolecular chiral aggregate consisting of two coaxial helices: the internal helix described by the allene stack and the external helix which consist in a 4-helix described by the four allene substituents. More precisely, this supramolecular aggregate possesses six axially chiral elements within its structure—the allene, the allene stack (internal helix) and the stacks of the four allene substituents (external 4-helix)—. Interestingly, slight variations in the magnitude of the tilting degree while keeping its <i>P</i>- or <i>M</i>- orientation (internal helix) can vary the orientation of the 4-axial motifs at the external helix. Thus, while (<i>P</i>)-<b>1</b> produces a supramolecular helix with a Θ ca. 15° (<i>P</i><sub>int</sub>) and a <i>M<sub>1</sub></i>/<i>P<sub>2</sub></i>/<i>M</i><sub><i>1’</i></sub>/<i>P</i><sub><i>2’</i></sub> orientation of the four axial motifs at the periphery, (<i>P</i>)-<b>2</b> produces a supramolecular helix with a Θ ca. 23° (<i>P</i><sub>int</sub>) and a <i>P<sub>1</sub></i>/<i>P<sub>2</sub></i>/<i>P</i><sub><i>1’</i></sub>/<i>P</i><sub><i>2’</i></sub> orientation of the four axial motifs at the external helix. As a result, the ECD spectra and the AFM images of the (<i>P</i>)-<b>1</b> and (<i>P</i>)-<b>2</b> supramolecular aggregates dominated by the 1 and 1’ substituents of the chiral allene indicate opposite handedness although the chirality of the building block and the orientation of the allene stack are the same</p>\",\"PeriodicalId\":125,\"journal\":{\"name\":\"Angewandte Chemie International Edition\",\"volume\":\"64 10\",\"pages\":\"\"},\"PeriodicalIF\":16.9000,\"publicationDate\":\"2024-12-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/anie.202421310\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Angewandte Chemie International Edition\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/anie.202421310\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Angewandte Chemie International Edition","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/anie.202421310","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Coaxial Helices in Chiral Supramolecular Aggregates from Highly Hindered Chiral Allenes
Chiral allenes self-assembly following a cooperative mechanism into a supramolecular chiral aggregate consisting of two coaxial helices: the internal helix described by the allene stack and the external helix which consist in a 4-helix described by the four allene substituents. More precisely, this supramolecular aggregate possesses six axially chiral elements within its structure—the allene, the allene stack (internal helix) and the stacks of the four allene substituents (external 4-helix)—. Interestingly, slight variations in the magnitude of the tilting degree while keeping its P- or M- orientation (internal helix) can vary the orientation of the 4-axial motifs at the external helix. Thus, while (P)-1 produces a supramolecular helix with a Θ ca. 15° (Pint) and a M1/P2/M1’/P2’ orientation of the four axial motifs at the periphery, (P)-2 produces a supramolecular helix with a Θ ca. 23° (Pint) and a P1/P2/P1’/P2’ orientation of the four axial motifs at the external helix. As a result, the ECD spectra and the AFM images of the (P)-1 and (P)-2 supramolecular aggregates dominated by the 1 and 1’ substituents of the chiral allene indicate opposite handedness although the chirality of the building block and the orientation of the allene stack are the same
期刊介绍:
Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.