饱和的碳氢键氧化是合成化学和化学工业中一类重要的化学反应.然而,饱和C(sp^(3))−H键离解能(BDEs)较高、极性较弱,导致了底物难以活化和催化转化效率较低等问题.在过去的几十年,C(sp^(3))−H键的定向活化转化取得了重要的进展.其中,关于...饱和的碳氢键氧化是合成化学和化学工业中一类重要的化学反应.然而,饱和C(sp^(3))−H键离解能(BDEs)较高、极性较弱,导致了底物难以活化和催化转化效率较低等问题.在过去的几十年,C(sp^(3))−H键的定向活化转化取得了重要的进展.其中,关于C(sp^(3))−H键催化氧化的研究主要涉及一些键能低的、预活化的C−H键,包括苄基型、亚甲基型、脂肪族X−CH_(2)(X=O,N)和甲苯等,含有未活化C(sp^(3))−H键的复杂化合物的选择性氧化仍具有挑战性.例如,芳基醚C(sp^(3))−H键功能化通常采用计量的过氧化物氧化剂,或者通过单电子氧化和碱促进的去质子化进一步构建C−C/C−N键,产物选择性较低,也带来了一些不利的环境影响.因此,有必要开发高效、温和的芳基醚C(sp^(3))−H键选择氧化方法,并将其应用于有机合成和药物开发.近年来,光催化C(sp^(3))−H键氧化因其操作简便、氧化还原中性等优点,已发展成为一种有用且多样的催化研究工具.本文发展了一种利用氧气作为氧化剂,在可见光驱动下选择性地将芳基醚C(sp^(3))−H键氧化成为甲酸苯酯类产物的新方法.使用Mes-10-phenyl-Acr^(+)−BF_(4)^(-)光催化剂,高效活化多种氯源(如盐酸、无机氯盐和有机氯化物)得到氯自由基,由于其具有较高的氧化能力(+2.03 V vs.SCE)和对氢原子的亲和力,能够通过氢原子转移过程活化芳基醚C(sp^(3))−键,攫取氢自由基得到相应的烷基碳自由基(•CH_(2)OPh)中间体,进一步被分子氧选择氧化得到酯类目标产物.研究结果表明,多种链状芳基醚和不同取代(如给电子基和吸电子基)芳基醚均可发生氧化反应,高收率地合成了一系列官能团丰富的甲酸苯酯类化合物.本文方法具有反应条件温和、操作简单、官能团耐受性好以及可规模化放大等优点,并且少量的水对反应没有明显影响.机理实验研究结果表明,芳基醚C(sp^(3))−H键的断裂是反应过程的决速步骤.紫外可见吸收光谱结果表明,氯离子与催化剂之间的相互作用强于底物,并且自由基捕获实验证实反应体系中存在氯自由基和烷基碳自由基物种,表明反应经历自由基路径.此外,电子顺磁共振测试结果表明,反应过程中存在单线态氧物种,可能是激发态的光催化剂直接与氧气发生能量转移得到;同位素实验(18O)揭示了甲酸苯酯类化合物氧的来源.综上,本文实现了温和条件下光催化芳基醚C(sp^(3))−H键选择氧化反应,高收率合成了一系列甲酸苯酯类化合物.该方法避免了化学计量的过氧化物和碱等添加剂的使用以及底物的过度氧化,阐明了催化反应机制,为其他醚类化合物的C(sp^(3))−H键氧化功能化提供了新思路,为后续化学合成和药物开发提供了参考和启示.展开更多
SP3 （simplified P3） theory is widely used in LWR （light water reactor） analyses to partly capture the transport effect, especially for pin-by-pin core analysis with pin size homogenization. In this paper, a SP3 co...SP3 （simplified P3） theory is widely used in LWR （light water reactor） analyses to partly capture the transport effect, especially for pin-by-pin core analysis with pin size homogenization. In this paper, a SP3 code named STELLA is developed and verified at SNERDI （Shanghai Nuclear Engineering Research and Design Institute）. For SP3 method, neutron transport equation can be transformed into two coupled equations in the same mathematical form as diffusion equation. In this work, SANM （semi-analytic nodal method） is used to solve diffusion-like equation, due to its easy to handle multi-group problem. Whole core nodal boundary net current coupling is used to improve convergence stability in SANM, instead of solving two-node problem. CMFD （coarse-mesh finite difference） acceleration method is employed for 0-th SP3 equation, which represents the neutron balance relationship. Three benchmarks are used to verify the SP3 code, STELLA. The first one is a self-defined one dimensional problem, which demonstrates SP3 method is extremely accurate, due to no academic approximation in one dimensional for SP3. The second one is a two dimensional one-group problem cited from Larsen＇s paper, which is usually used to verify and prove the SP3 code correct and accurate. And the third one is modified from 2D C5G7-MOX benchmark, whose numerical results indicate that STELLA is accurate and efficient in pin size level, compared to diffusion model.展开更多
The development of practical methods for the direct and selective C(sp^(3))‒H functionalization of hydrocarbons is an attractive topic in synthetic chemistry.Although the radical‐mediated hydrogen atom transfer(HAT)p...The development of practical methods for the direct and selective C(sp^(3))‒H functionalization of hydrocarbons is an attractive topic in synthetic chemistry.Although the radical‐mediated hydrogen atom transfer(HAT)process has shown considerable potential in such reactions,it still faces fundamental problems associated with reactivity and selectivity.Herein,we report a convenient and economic approach to site‐selective C(sp^(3))‒H sulfonylation via photo‐induced HAT catalysis.Employing a conjugated polycyclic quinone as a direct HAT photocatalyst,commercially available inorganic sulfinates as the sulfonylation source,copper triflate as an inexpensive oxidant,a variety of toluene derivatives and cycloalkanes were converted into biologically and synthetically interesting sulfone products under mild conditions.The mechanistic studies reveal that the reaction sequence involves direct HAT‐induced radical formation and a subsequent copper‐mediated organometallic process for the C‒S bond formation.This method offers an appealing opportunity to furnish high value‐added products from abundant hydrocarbon starting materials and inexpensive reagents.展开更多
3d-Metal-catalyzed tertiary C(sp^(3))–H bond activation has been a formidable challenge.Herein,a tertiary C(sp^(3))–H bond is smoothly activated by Ni–Al bimetallic catalysts for dual C–H annulation of formamides ...3d-Metal-catalyzed tertiary C(sp^(3))–H bond activation has been a formidable challenge.Herein,a tertiary C(sp^(3))–H bond is smoothly activated by Ni–Al bimetallic catalysts for dual C–H annulation of formamides with alkynes,delivering a series of δ-lactams with a quaternary carbon up to 98%yield.Various tertiary C(sp^(3))–H bonds such as noncyclic,monocyclic and bridged-ring tertiary C(sp^(3))–H bonds are all compatible with the reaction.展开更多
Converting hydrocarbons into aldehydes in a green and environmentally benign way is of great signif-icance in fine chemistry.In this work,all-inorganic Cs_(3)Bi_(2)B_(9) perovskite nanoparticles were uniformly loaded ...Converting hydrocarbons into aldehydes in a green and environmentally benign way is of great signif-icance in fine chemistry.In this work,all-inorganic Cs_(3)Bi_(2)B_(9) perovskite nanoparticles were uniformly loaded on BiOBr nanosheets via an in-situ growth method,which can selectivity photoactivate aromatic C(sp3)-H bond of toluene to generate benzaldehyde.According to the in-situ X-ray photoelectron spec-troscopy characterization,the photogenerated electrons of BiOBr transfer to Cs_(3)Bi_(2)B_(9) enforced by the in-ternal electric field under light irradiation,resulting in S-scheme heterojunction.Furthermore,theoretical calculations indicate that toluene molecules are inclined to adsorb on the BiOBr surface,subsequently in-volving the oxidation reaction to generate benzyl radical(PhCH_(2)·)by using the energetic holes of BiOBr,while the remaining photoinduced electrons in the conduction band(CB)of Cs_(3)Bi_(2)B_(9) with powerful reduction ability reduce O2 into·O_(2)^(-),which is the vital oxidative active species working on toluene selective oxidation process.Such an unexceptionable charge carrier utilization mode and tendentious ad-sorption behavior of reactants contribute to the optimized Cs_(3)Bi_(2)B_(9)/BiOBr heterojunction with excellent photocatalytic performance,achieving a maximum of 22.5%toluene conversion and 96.2%selectivity to-wards benzaldehyde formation.This work provides a rational photocatalyst heterojunction construction protocol for the selective oxidation of saturated aromatic C-H bonds.展开更多
The first catalytic enantioselective C（sp）-C（sp^3） cross-coupling reaction between N-tosylhydrazones and trialkylsilylethynes in the presence of Cu（I） salts and chiral phosphoramidite ligands was developed. A se...The first catalytic enantioselective C（sp）-C（sp^3） cross-coupling reaction between N-tosylhydrazones and trialkylsilylethynes in the presence of Cu（I） salts and chiral phosphoramidite ligands was developed. A series of svnthetically interesting, functionalized alkynes were obtained with moderate to good enanttiselectivities （up to 83% ee）. Cu（ll） carbene migratory insertion is proposed to be the enantio-determining step. KEYWORDS C（sp）--C（sp^3） cross-coupling, metal carbene, asymmetric catalysis, Cu（I） catalysts, N-tosylhydrazones展开更多
文摘饱和的碳氢键氧化是合成化学和化学工业中一类重要的化学反应.然而,饱和C(sp^(3))−H键离解能(BDEs)较高、极性较弱,导致了底物难以活化和催化转化效率较低等问题.在过去的几十年,C(sp^(3))−H键的定向活化转化取得了重要的进展.其中,关于C(sp^(3))−H键催化氧化的研究主要涉及一些键能低的、预活化的C−H键,包括苄基型、亚甲基型、脂肪族X−CH_(2)(X=O,N)和甲苯等,含有未活化C(sp^(3))−H键的复杂化合物的选择性氧化仍具有挑战性.例如,芳基醚C(sp^(3))−H键功能化通常采用计量的过氧化物氧化剂,或者通过单电子氧化和碱促进的去质子化进一步构建C−C/C−N键,产物选择性较低,也带来了一些不利的环境影响.因此,有必要开发高效、温和的芳基醚C(sp^(3))−H键选择氧化方法,并将其应用于有机合成和药物开发.近年来,光催化C(sp^(3))−H键氧化因其操作简便、氧化还原中性等优点,已发展成为一种有用且多样的催化研究工具.本文发展了一种利用氧气作为氧化剂,在可见光驱动下选择性地将芳基醚C(sp^(3))−H键氧化成为甲酸苯酯类产物的新方法.使用Mes-10-phenyl-Acr^(+)−BF_(4)^(-)光催化剂,高效活化多种氯源(如盐酸、无机氯盐和有机氯化物)得到氯自由基,由于其具有较高的氧化能力(+2.03 V vs.SCE)和对氢原子的亲和力,能够通过氢原子转移过程活化芳基醚C(sp^(3))−键,攫取氢自由基得到相应的烷基碳自由基(•CH_(2)OPh)中间体,进一步被分子氧选择氧化得到酯类目标产物.研究结果表明,多种链状芳基醚和不同取代(如给电子基和吸电子基)芳基醚均可发生氧化反应,高收率地合成了一系列官能团丰富的甲酸苯酯类化合物.本文方法具有反应条件温和、操作简单、官能团耐受性好以及可规模化放大等优点,并且少量的水对反应没有明显影响.机理实验研究结果表明,芳基醚C(sp^(3))−H键的断裂是反应过程的决速步骤.紫外可见吸收光谱结果表明,氯离子与催化剂之间的相互作用强于底物,并且自由基捕获实验证实反应体系中存在氯自由基和烷基碳自由基物种,表明反应经历自由基路径.此外,电子顺磁共振测试结果表明,反应过程中存在单线态氧物种,可能是激发态的光催化剂直接与氧气发生能量转移得到;同位素实验(18O)揭示了甲酸苯酯类化合物氧的来源.综上,本文实现了温和条件下光催化芳基醚C(sp^(3))−H键选择氧化反应,高收率合成了一系列甲酸苯酯类化合物.该方法避免了化学计量的过氧化物和碱等添加剂的使用以及底物的过度氧化,阐明了催化反应机制,为其他醚类化合物的C(sp^(3))−H键氧化功能化提供了新思路,为后续化学合成和药物开发提供了参考和启示.
文摘SP3 （simplified P3） theory is widely used in LWR （light water reactor） analyses to partly capture the transport effect, especially for pin-by-pin core analysis with pin size homogenization. In this paper, a SP3 code named STELLA is developed and verified at SNERDI （Shanghai Nuclear Engineering Research and Design Institute）. For SP3 method, neutron transport equation can be transformed into two coupled equations in the same mathematical form as diffusion equation. In this work, SANM （semi-analytic nodal method） is used to solve diffusion-like equation, due to its easy to handle multi-group problem. Whole core nodal boundary net current coupling is used to improve convergence stability in SANM, instead of solving two-node problem. CMFD （coarse-mesh finite difference） acceleration method is employed for 0-th SP3 equation, which represents the neutron balance relationship. Three benchmarks are used to verify the SP3 code, STELLA. The first one is a self-defined one dimensional problem, which demonstrates SP3 method is extremely accurate, due to no academic approximation in one dimensional for SP3. The second one is a two dimensional one-group problem cited from Larsen＇s paper, which is usually used to verify and prove the SP3 code correct and accurate. And the third one is modified from 2D C5G7-MOX benchmark, whose numerical results indicate that STELLA is accurate and efficient in pin size level, compared to diffusion model.
文摘The development of practical methods for the direct and selective C(sp^(3))‒H functionalization of hydrocarbons is an attractive topic in synthetic chemistry.Although the radical‐mediated hydrogen atom transfer(HAT)process has shown considerable potential in such reactions,it still faces fundamental problems associated with reactivity and selectivity.Herein,we report a convenient and economic approach to site‐selective C(sp^(3))‒H sulfonylation via photo‐induced HAT catalysis.Employing a conjugated polycyclic quinone as a direct HAT photocatalyst,commercially available inorganic sulfinates as the sulfonylation source,copper triflate as an inexpensive oxidant,a variety of toluene derivatives and cycloalkanes were converted into biologically and synthetically interesting sulfone products under mild conditions.The mechanistic studies reveal that the reaction sequence involves direct HAT‐induced radical formation and a subsequent copper‐mediated organometallic process for the C‒S bond formation.This method offers an appealing opportunity to furnish high value‐added products from abundant hydrocarbon starting materials and inexpensive reagents.
基金the National Key R&D Program of China(grant no.2022YFA1504300)the National Natural Science Foundation of China(grant nos.22188101 and 22325103)+1 种基金the Haihe Laboratory of Sustainable Chemical Transformations and“Frontiers Science Center for New Organic Matter,”Nankai University(grant no.63181206)the Fundamental Research Funds for the Central Universities for financial support.
文摘3d-Metal-catalyzed tertiary C(sp^(3))–H bond activation has been a formidable challenge.Herein,a tertiary C(sp^(3))–H bond is smoothly activated by Ni–Al bimetallic catalysts for dual C–H annulation of formamides with alkynes,delivering a series of δ-lactams with a quaternary carbon up to 98%yield.Various tertiary C(sp^(3))–H bonds such as noncyclic,monocyclic and bridged-ring tertiary C(sp^(3))–H bonds are all compatible with the reaction.
基金National Natural Science Foundation of China(Nos.21905209,52171145,and 51973078)Natural Science Foundation of Xinjiang Uygur Autonomous Region(No.2020D01B25).
文摘Converting hydrocarbons into aldehydes in a green and environmentally benign way is of great signif-icance in fine chemistry.In this work,all-inorganic Cs_(3)Bi_(2)B_(9) perovskite nanoparticles were uniformly loaded on BiOBr nanosheets via an in-situ growth method,which can selectivity photoactivate aromatic C(sp3)-H bond of toluene to generate benzaldehyde.According to the in-situ X-ray photoelectron spec-troscopy characterization,the photogenerated electrons of BiOBr transfer to Cs_(3)Bi_(2)B_(9) enforced by the in-ternal electric field under light irradiation,resulting in S-scheme heterojunction.Furthermore,theoretical calculations indicate that toluene molecules are inclined to adsorb on the BiOBr surface,subsequently in-volving the oxidation reaction to generate benzyl radical(PhCH_(2)·)by using the energetic holes of BiOBr,while the remaining photoinduced electrons in the conduction band(CB)of Cs_(3)Bi_(2)B_(9) with powerful reduction ability reduce O2 into·O_(2)^(-),which is the vital oxidative active species working on toluene selective oxidation process.Such an unexceptionable charge carrier utilization mode and tendentious ad-sorption behavior of reactants contribute to the optimized Cs_(3)Bi_(2)B_(9)/BiOBr heterojunction with excellent photocatalytic performance,achieving a maximum of 22.5%toluene conversion and 96.2%selectivity to-wards benzaldehyde formation.This work provides a rational photocatalyst heterojunction construction protocol for the selective oxidation of saturated aromatic C-H bonds.
基金Acknowledgement The project is supported by the National Basic Research Program of China （973 Program, No. 2015CB856600）, the National Natural Science Foundation of China （Grant 21472004, 21332002） and the China Postdoctoral Science Foundation Funded Project （2015M5B0911）.
文摘The first catalytic enantioselective C（sp）-C（sp^3） cross-coupling reaction between N-tosylhydrazones and trialkylsilylethynes in the presence of Cu（I） salts and chiral phosphoramidite ligands was developed. A series of svnthetically interesting, functionalized alkynes were obtained with moderate to good enanttiselectivities （up to 83% ee）. Cu（ll） carbene migratory insertion is proposed to be the enantio-determining step. KEYWORDS C（sp）--C（sp^3） cross-coupling, metal carbene, asymmetric catalysis, Cu（I） catalysts, N-tosylhydrazones
