Suppr超能文献

追踪铁配合物中激发态电荷和自旋动力学。

Tracking excited-state charge and spin dynamics in iron coordination complexes.

机构信息

PULSE Institute, SLAC National Accelerator Laboratory, Stanford University, Stanford, California 94305, USA.

LCLS, SLAC National Accelerator Laboratory, Menlo Park, California 94025, USA.

出版信息

Nature. 2014 May 15;509(7500):345-8. doi: 10.1038/nature13252. Epub 2014 May 7.

Abstract

Crucial to many light-driven processes in transition metal complexes is the absorption and dissipation of energy by 3d electrons. But a detailed understanding of such non-equilibrium excited-state dynamics and their interplay with structural changes is challenging: a multitude of excited states and possible transitions result in phenomena too complex to unravel when faced with the indirect sensitivity of optical spectroscopy to spin dynamics and the flux limitations of ultrafast X-ray sources. Such a situation exists for archetypal polypyridyl iron complexes, such as Fe(2,2'-bipyridine)3, where the excited-state charge and spin dynamics involved in the transition from a low- to a high-spin state (spin crossover) have long been a source of interest and controversy. Here we demonstrate that femtosecond resolution X-ray fluorescence spectroscopy, with its sensitivity to spin state, can elucidate the spin crossover dynamics of Fe(2,2'-bipyridine)3 on photoinduced metal-to-ligand charge transfer excitation. We are able to track the charge and spin dynamics, and establish the critical role of intermediate spin states in the crossover mechanism. We anticipate that these capabilities will make our method a valuable tool for mapping in unprecedented detail the fundamental electronic excited-state dynamics that underpin many useful light-triggered molecular phenomena involving 3d transition metal complexes.

摘要

对于过渡金属配合物中的许多光驱动过程而言,3d 电子的能量吸收和耗散至关重要。但是,详细了解这种非平衡激发态动力学及其与结构变化的相互作用具有挑战性:大量的激发态和可能的跃迁导致了在面对光学光谱对自旋动力学的间接灵敏度和超快 X 射线源通量限制时过于复杂而无法解决的现象。这种情况存在于典型的多吡啶铁配合物中,例如 Fe(2,2'-bipyridine)3,其中涉及从低自旋态到高自旋态(自旋交叉)的激发态电荷和自旋动力学一直是人们关注和争议的来源。在这里,我们证明飞秒分辨率 X 射线荧光光谱法对自旋态的灵敏度可以阐明 Fe(2,2'-bipyridine)3 在光诱导的金属-配体电荷转移激发下的自旋交叉动力学。我们能够跟踪电荷和自旋动力学,并确定中间自旋态在交叉机制中的关键作用。我们预计这些功能将使我们的方法成为一种有价值的工具,可以以前所未有的细节绘制基本的电子激发态动力学图谱,这些动力学图谱是许多涉及 3d 过渡金属配合物的有用光触发分子现象的基础。

相似文献

1
Tracking excited-state charge and spin dynamics in iron coordination complexes.
Nature. 2014 May 15;509(7500):345-8. doi: 10.1038/nature13252. Epub 2014 May 7.
4
Mechanistic studies of photoinduced spin crossover and electron transfer in inorganic complexes.
Acc Chem Res. 2015 Apr 21;48(4):1140-8. doi: 10.1021/ar500407p. Epub 2015 Mar 19.
6
Ligand manipulation of charge transfer excited state relaxation and spin crossover in [Fe(2,2'-bipyridine)(CN)].
Struct Dyn. 2017 Jun 6;4(4):044030. doi: 10.1063/1.4985017. eCollection 2017 Jul.
8
Ultrafast Spin Crossover in [Fe (bpy) ] : Revealing Two Competing Mechanisms by Extreme Ultraviolet Photoemission Spectroscopy.
Chemphyschem. 2017 Mar 3;18(5):465-469. doi: 10.1002/cphc.201601396. Epub 2017 Jan 19.
10
Spin-vibronic quantum dynamics for ultrafast excited-state processes.
Acc Chem Res. 2015 Mar 17;48(3):809-17. doi: 10.1021/ar500369r. Epub 2015 Feb 3.

引用本文的文献

1
Ultrafast Optical Pump-Hard X-Ray Probe Spectroscopy of Transition Metal Complexes in Solution at SLAC.
Synchrotron Radiat News. 2025 May-Jun;38(3):31-37. doi: 10.1080/08940886.2025.2501889. Epub 2025 May 22.
3
Ultrafast charge-transfer-induced spin transition in cobalt-tungstate molecular photomagnets.
Nat Commun. 2025 Jun 6;16(1):5012. doi: 10.1038/s41467-025-60401-4.
4
Capturing Ultrafast Spin Dynamics in Single-Molecule Magnets Using Femtosecond X-ray Emission Spectroscopy.
J Phys Chem Lett. 2025 May 1;16(17):4148-4154. doi: 10.1021/acs.jpclett.5c00383. Epub 2025 Apr 17.
5
A high-energy Laue X-ray emission spectrometer at the FXE instrument at the European XFEL.
J Synchrotron Radiat. 2025 May 1;32(Pt 3):506-523. doi: 10.1107/S1600577525001389. Epub 2025 Mar 31.
7
Simulation of Ultrafast Excited-State Dynamics in Fe(II) Complexes: Assessment of Electronic Structure Descriptions.
J Chem Theory Comput. 2025 Jan 28;21(2):560-574. doi: 10.1021/acs.jctc.4c01331. Epub 2025 Jan 3.
8
Size and Surface Effects in the Ultrafast Dynamics of Strongly Cooperative Spin-Crossover Nanoparticles.
Small. 2025 Jan;21(2):e2405571. doi: 10.1002/smll.202405571. Epub 2024 Nov 10.
9
Structure and spin of the low- and high-spin states of Fe(phen) studied by x-ray scattering and emission spectroscopy.
Struct Dyn. 2024 Oct 23;11(5):054901. doi: 10.1063/4.0000254. eCollection 2024 Sep.

本文引用的文献

2
Ultrafast deactivation mechanism of the excited singlet in the light-induced spin crossover of [Fe(2,2'-bipyridine)3]2+.
Chemistry. 2013 Dec 16;19(51):17541-51. doi: 10.1002/chem.201302992. Epub 2013 Nov 7.
3
Femtosecond X-ray absorption spectroscopy at a hard X-ray free electron laser: application to spin crossover dynamics.
J Phys Chem A. 2013 Jan 31;117(4):735-40. doi: 10.1021/jp312559h. Epub 2013 Jan 17.
5
A multi-crystal wavelength dispersive x-ray spectrometer.
Rev Sci Instrum. 2012 Jul;83(7):073114. doi: 10.1063/1.4737630.
6
Spectral encoding of x-ray/optical relative delay.
Opt Express. 2011 Oct 24;19(22):21855-65. doi: 10.1364/OE.19.021855.
7
Picosecond time-resolved X-ray emission spectroscopy: ultrafast spin-state determination in an iron complex.
Angew Chem Int Ed Engl. 2010 Aug 9;49(34):5910-2. doi: 10.1002/anie.201000844.
8
Probing valence orbital composition with iron Kbeta X-ray emission spectroscopy.
J Am Chem Soc. 2010 Jul 21;132(28):9715-27. doi: 10.1021/ja101281e.
9
Study of the light-induced spin crossover process of the [Fe(II)(bpy)3]2+ complex.
Chemistry. 2010 Apr 19;16(15):4550-6. doi: 10.1002/chem.200903423. Epub 2010 Mar 12.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验