{"title":"调节Hf-PCN-224(M)对β-羰基C(sp3)-氢键激活和双官能化的带结构:通过光氧化还原串联C(sp3)自由基交叉偶联","authors":"Lingjuan Zhang , Lijuan Ma , Jincong Yuan , Xian-Ming Zhang , Zhiyong Tang","doi":"10.1016/j.apcatb.2022.122049","DOIUrl":null,"url":null,"abstract":"<div><p>The construction of C(sp<sup>3</sup>)-C(sp<sup>3</sup>) bonds by different C(sp<sup>3</sup>) radicals coupling reactions is still unexplored due to the high bond dissociation energy of C(sp<sup>3</sup>)-H bond and the difficulty for selective generating of C(sp<sup>3</sup>) radical. Benefiting from the precisely regulating for band structures of Hf-PCN-224(M), the β-carbonyl C(sp<sup>3</sup>)-H bonds are effectively oxidized by photo-generated holes to affording C(sp<sup>3</sup>) radicals in this work. C(sp<sup>3</sup>)-C(sp<sup>3</sup>) and C(sp<sup>3</sup>)-O bonds are constructed by tandem radical-radical cross-coupling, hydrogen atom transfer (HAT), and radical-radical cross-coupling between two C(sp<sup>3</sup>)-H bonds, enabling an effective C<sub>3</sub>-difunctionalization of indolin-2-ones under photo-thermo synergetic catalysis on Hf-PCN-224(Cu). Significantly, OH serves as triple roles: introduced hydroxyl group in situ, HAT abstractor and α-heteroatom for secondary activating C(sp<sup>3</sup>)-H bonds. Control experiments, EPR spectroscopy and DFT calculation provide insight into the tandem radicals cross-coupling mechanism. This operable strategy opens up a door for the difunctionalization of C(sp<sup>3</sup>)-H bonds in heterogeneous photoredox manner.</p></div>","PeriodicalId":244,"journal":{"name":"Applied Catalysis B: Environmental","volume":"321 ","pages":"Article 122049"},"PeriodicalIF":20.2000,"publicationDate":"2023-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tuning band structures of Hf-PCN-224(M) for β-Carbonyl C(sp3)-H bond activation and difunctionalization: Tandem C(sp3) radical cross-coupling through photoredox\",\"authors\":\"Lingjuan Zhang , Lijuan Ma , Jincong Yuan , Xian-Ming Zhang , Zhiyong Tang\",\"doi\":\"10.1016/j.apcatb.2022.122049\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The construction of C(sp<sup>3</sup>)-C(sp<sup>3</sup>) bonds by different C(sp<sup>3</sup>) radicals coupling reactions is still unexplored due to the high bond dissociation energy of C(sp<sup>3</sup>)-H bond and the difficulty for selective generating of C(sp<sup>3</sup>) radical. Benefiting from the precisely regulating for band structures of Hf-PCN-224(M), the β-carbonyl C(sp<sup>3</sup>)-H bonds are effectively oxidized by photo-generated holes to affording C(sp<sup>3</sup>) radicals in this work. C(sp<sup>3</sup>)-C(sp<sup>3</sup>) and C(sp<sup>3</sup>)-O bonds are constructed by tandem radical-radical cross-coupling, hydrogen atom transfer (HAT), and radical-radical cross-coupling between two C(sp<sup>3</sup>)-H bonds, enabling an effective C<sub>3</sub>-difunctionalization of indolin-2-ones under photo-thermo synergetic catalysis on Hf-PCN-224(Cu). Significantly, OH serves as triple roles: introduced hydroxyl group in situ, HAT abstractor and α-heteroatom for secondary activating C(sp<sup>3</sup>)-H bonds. Control experiments, EPR spectroscopy and DFT calculation provide insight into the tandem radicals cross-coupling mechanism. This operable strategy opens up a door for the difunctionalization of C(sp<sup>3</sup>)-H bonds in heterogeneous photoredox manner.</p></div>\",\"PeriodicalId\":244,\"journal\":{\"name\":\"Applied Catalysis B: Environmental\",\"volume\":\"321 \",\"pages\":\"Article 122049\"},\"PeriodicalIF\":20.2000,\"publicationDate\":\"2023-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Catalysis B: Environmental\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0926337322009900\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Catalysis B: Environmental","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0926337322009900","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Tuning band structures of Hf-PCN-224(M) for β-Carbonyl C(sp3)-H bond activation and difunctionalization: Tandem C(sp3) radical cross-coupling through photoredox
The construction of C(sp3)-C(sp3) bonds by different C(sp3) radicals coupling reactions is still unexplored due to the high bond dissociation energy of C(sp3)-H bond and the difficulty for selective generating of C(sp3) radical. Benefiting from the precisely regulating for band structures of Hf-PCN-224(M), the β-carbonyl C(sp3)-H bonds are effectively oxidized by photo-generated holes to affording C(sp3) radicals in this work. C(sp3)-C(sp3) and C(sp3)-O bonds are constructed by tandem radical-radical cross-coupling, hydrogen atom transfer (HAT), and radical-radical cross-coupling between two C(sp3)-H bonds, enabling an effective C3-difunctionalization of indolin-2-ones under photo-thermo synergetic catalysis on Hf-PCN-224(Cu). Significantly, OH serves as triple roles: introduced hydroxyl group in situ, HAT abstractor and α-heteroatom for secondary activating C(sp3)-H bonds. Control experiments, EPR spectroscopy and DFT calculation provide insight into the tandem radicals cross-coupling mechanism. This operable strategy opens up a door for the difunctionalization of C(sp3)-H bonds in heterogeneous photoredox manner.
期刊介绍:
Applied Catalysis B: Environment and Energy (formerly Applied Catalysis B: Environmental) is a journal that focuses on the transition towards cleaner and more sustainable energy sources. The journal's publications cover a wide range of topics, including:
1.Catalytic elimination of environmental pollutants such as nitrogen oxides, carbon monoxide, sulfur compounds, chlorinated and other organic compounds, and soot emitted from stationary or mobile sources.
2.Basic understanding of catalysts used in environmental pollution abatement, particularly in industrial processes.
3.All aspects of preparation, characterization, activation, deactivation, and regeneration of novel and commercially applicable environmental catalysts.
4.New catalytic routes and processes for the production of clean energy, such as hydrogen generation via catalytic fuel processing, and new catalysts and electrocatalysts for fuel cells.
5.Catalytic reactions that convert wastes into useful products.
6.Clean manufacturing techniques that replace toxic chemicals with environmentally friendly catalysts.
7.Scientific aspects of photocatalytic processes and a basic understanding of photocatalysts as applied to environmental problems.
8.New catalytic combustion technologies and catalysts.
9.New catalytic non-enzymatic transformations of biomass components.
The journal is abstracted and indexed in API Abstracts, Research Alert, Chemical Abstracts, Web of Science, Theoretical Chemical Engineering Abstracts, Engineering, Technology & Applied Sciences, and others.