• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

时间分辨多探针光谱学

Time-resolved multiple probe spectroscopy.

作者信息

Greetham G M, Sole D, Clark I P, Parker A W, Pollard M R, Towrie M

机构信息

Central Laser Facility, Science and Technology Facilities Council, Research Complex at Harwell, Rutherford Appleton Laboratory, Harwell, Oxfordshire, OX11 0QX, United Kingdom.

出版信息

Rev Sci Instrum. 2012 Oct;83(10):103107. doi: 10.1063/1.4758999.

DOI:10.1063/1.4758999
PMID:23126751
Abstract

Time-resolved multiple probe spectroscopy combines optical, electronic, and data acquisition capabilities to enable measurement of picosecond to millisecond time-resolved spectra within a single experiment, using a single activation pulse. This technology enables a wide range of dynamic processes to be studied on a single laser and sample system. The technique includes a 1 kHz pump, 10 kHz probe flash photolysis-like mode of acquisition (pump-probe-probe-probe, etc.), increasing the amount of information from each experiment. We demonstrate the capability of the instrument by measuring the photolysis of tungsten hexacarbonyl (W(CO)(6)) monitored by IR absorption spectroscopy, following picosecond vibrational cooling of product formation through to slower bimolecular diffusion reactions on the microsecond time scale.

摘要

时间分辨多探针光谱技术结合了光学、电子和数据采集能力,能够在单次实验中使用单个激活脉冲测量皮秒到毫秒时间分辨光谱。该技术可在单个激光和样品系统上研究广泛的动态过程。该技术包括1 kHz泵浦、10 kHz探针的类似闪光光解的采集模式(泵浦-探针-探针-探针等),增加了每次实验的信息量。我们通过测量六羰基钨(W(CO)₆)的光解来展示该仪器的能力,通过红外吸收光谱监测,从皮秒级的产物形成振动冷却到微秒时间尺度上较慢分子扩散反应。

相似文献

1
Time-resolved multiple probe spectroscopy.时间分辨多探针光谱学
Rev Sci Instrum. 2012 Oct;83(10):103107. doi: 10.1063/1.4758999.
2
Ultra-broadband infrared pump-probe spectroscopy using synchrotron radiation and a tuneable pump.利用同步辐射和可调谐泵浦的超宽带红外泵浦-探测光谱学。
Rev Sci Instrum. 2011 Jun;82(6):063101. doi: 10.1063/1.3592332.
3
Mid-infrared picosecond pump-dump-probe and pump-repump-probe experiments to resolve a ground-state intermediate in cyanobacterial phytochrome Cph1.中红外皮秒泵-探测和泵-重探测实验解析蓝细菌光敏色素 Cph1 的基态中间产物。
J Phys Chem B. 2009 Dec 24;113(51):16354-64. doi: 10.1021/jp9038539.
4
A 100 kHz Time-Resolved Multiple-Probe Femtosecond to Second Infrared Absorption Spectrometer.一台100千赫兹时间分辨多探针飞秒至秒红外吸收光谱仪。
Appl Spectrosc. 2016 Apr;70(4):645-53. doi: 10.1177/0003702816631302. Epub 2016 Feb 17.
5
Vibrational dynamics of hydrogen-bonded complexes in solutions studied with ultrafast infrared pump-probe spectroscopy.溶液中氢键复合物的超快红外泵浦探针光谱研究中的振动动力学。
Acc Chem Res. 2009 Sep 15;42(9):1259-69. doi: 10.1021/ar9000229.
6
Vibrational energy relaxation of benzene dimer and trimer in the CH stretching region studied by picosecond time-resolved IR-UV pump-probe spectroscopy.通过皮秒时间分辨红外-紫外泵浦探针光谱研究 CH 伸缩区域中苯二聚体和三聚体的振动能量弛豫。
J Chem Phys. 2012 Jan 28;136(4):044304. doi: 10.1063/1.3676658.
7
Development of a simultaneously frequency- and time-resolved Raman-induced Kerr effect probe.一种同时具有频率和时间分辨能力的拉曼诱导克尔效应探针的研制。
J Phys Chem A. 2009 Jan 8;113(1):135-40. doi: 10.1021/jp804283s.
8
Probing with randomly interleaved pulse train bridges the gap between ultrafast pump-probe and nanosecond flash photolysis.用随机交错脉冲序列进行探测弥合了超快泵浦-探测与纳秒闪光光解之间的差距。
Opt Lett. 2016 Apr 1;41(7):1498-501. doi: 10.1364/OL.41.001498.
9
Picosecond IR-UV pump-probe study on the vibrational relaxation of phenol-ethylene hydrogen-bonded cluster: difference of relaxation route/rate between the donor and the acceptor site excitations.皮秒红外-紫外泵浦-探测研究:苯酚-乙烯氢键簇的振动弛豫——供体和受体位点激发之间弛豫路径/速率的差异
J Phys Chem A. 2006 May 18;110(19):6250-5. doi: 10.1021/jp0571832.
10
Development of a multiplex fast-scan system for ultrafast time-resolved spectroscopy.用于超快时间分辨光谱学的多路复用快速扫描系统的开发。
Rev Sci Instrum. 2010 Jun;81(6):063110. doi: 10.1063/1.3455809.

引用本文的文献

1
Ultrafast photophysics of a positive reversibly switchable fluorescent protein.一种正向可逆切换荧光蛋白的超快光物理特性
Chem Sci. 2025 Aug 7. doi: 10.1039/d5sc04491j.
2
Dynamic Equilibrium between the Fluorescent State of Tryptophan and Its Cation-Electron Ion Pair Governs Triplet State Population.色氨酸荧光态与其阳离子-电子离子对之间的动态平衡决定了三重态布居数。
J Am Chem Soc. 2025 Sep 3;147(35):32064-32076. doi: 10.1021/jacs.5c10445. Epub 2025 Aug 21.
3
Direct observation of two-channel photodissociation of carbon monoxide from the hemoglobin subunits.
直接观察一氧化碳从血红蛋白亚基的双通道光解离。
Nat Commun. 2025 Aug 20;16(1):7746. doi: 10.1038/s41467-025-63092-z.
4
Photophysical and Time-resolved Infrared Properties of Long-Lived Rhenium(I) 4,5-Diazafluorene Tricarbonyl Chromophores.长寿命铼(I)4,5-二氮芴三羰基发色团的光物理和时间分辨红外性质
Chemphyschem. 2025 May 5;26(9):e202500008. doi: 10.1002/cphc.202500008. Epub 2025 Feb 23.
5
Probing the Signal Transduction Mechanism of the Light-Activated Adenylate Cyclase OaPAC Using Unnatural Amino Acid Mutagenesis.利用非天然氨基酸诱变探究光激活腺苷酸环化酶OaPAC的信号转导机制
ACS Chem Biol. 2025 Feb 21;20(2):369-377. doi: 10.1021/acschembio.4c00627. Epub 2025 Jan 22.
6
Enhancing Proton-Coupled Electron Transfer in Blue Light Using FAD Photoreceptor AppA.利用黄素腺嘌呤二核苷酸光感受器AppA增强蓝光中的质子耦合电子转移
J Am Chem Soc. 2025 Jan 8;147(1):39-44. doi: 10.1021/jacs.4c11817. Epub 2024 Dec 20.
7
Femtosecond to Microsecond Observation of Photochemical Pathways in Nitroaromatic Phototriggers Using Transient Absorption Spectroscopy.利用瞬态吸收光谱对硝基芳烃光引发剂中光化学途径进行飞秒至微秒级观测。
J Phys Chem A. 2024 Jul 25;128(29):5892-5905. doi: 10.1021/acs.jpca.4c02482. Epub 2024 Jul 11.
8
Unraveling the Ultrafast Photochemical Dynamics of Nitrobenzene in Aqueous Solution.解析硝基苯在水溶液中的超快光化学动力学
J Am Chem Soc. 2024 Apr 17;146(15):10407-10417. doi: 10.1021/jacs.3c13826. Epub 2024 Apr 4.
9
Laser induced temperature-jump time resolved IR spectroscopy of zeolites.沸石的激光诱导温度跃升时间分辨红外光谱学。
Chem Sci. 2024 Feb 7;15(10):3453-3465. doi: 10.1039/d3sc06128k. eCollection 2024 Mar 6.
10
Unveiling Mechanistic Complexity in Manganese-Catalyzed C-H Bond Functionalization Using IR Spectroscopy Over 16 Orders of Magnitude in Time.利用红外光谱在16个数量级的时间范围内揭示锰催化C-H键官能化的机理复杂性
Acc Chem Res. 2024 Mar 19;57(6):919-932. doi: 10.1021/acs.accounts.3c00774. Epub 2024 Feb 27.