Photodissociation dynamics of bromoiodomethane from the first and second absorption bands. A combined velocity map and slice imaging study
文献信息
David V. Chicharro, Eduardo Navarro, Luis Rubio-Lago, Luis Bañares
The photodissociation dynamics of bromoiodomethane (CH2BrI) have been investigated at the maximum of the first A and second A′ absorption bands, at 266 and 210 nm excitation wavelengths, respectively, using velocity map and slice imaging techniques in combination with a probe detection of both iodine and bromine fragments, I(2P3/2), I*(2P1/2), Br(2P3/2) and Br*(2P1/2) via (2 + 1) resonance enhanced multiphoton ionization. Experimental results, i.e. translational energy and angular distributions, are reported and discussed in conjunction with high level ab initio calculations of potential energy curves and absorption spectra. The results indicate that in the A-band, direct dissociation through the 5A′ excited state leads to the I(2P3/2) channel while I*(2P1/2) atoms are produced via the 5A′ → 4A′/4A′′ nonadiabatic crossing. The presence of Br and Br* fragments upon excitation to the A-band is attributed to indirect dissociation via a curve crossing between the 5A′ with upper excited states such as the 9A′. The A′-band is characterized by a strong photoselectivity leading exclusively to the Br(2P3/2) and Br*(2P1/2) channels, which are likely produced by dissociation through the 9A′ excited state. Avoided crossings between several excited states from both the A and A′ bands entangle however the possible reaction pathways.
期刊推荐

Russian Journal of Coordination Chemistry

New Journal of Chemistry

Organic Process Research & Development

Saudi Pharmaceutical Journal

Nature Medicine

Journal of Peptide Science

Journal of Saudi Chemical Society

Current Opinion in Solid State & Materials Science

Journal of Natural Medicines

Chemistry Education Research and Practice
相关文献
Interaction between probe molecules and zeolites. Part I: Pair-wise addition scheme applied to the calculation of the interaction energy of CO and N2 adsorbed in Na4Ca4A
A. V. Larin, L. Leherte, D. P. Vercauteren
DOI: 10.1039/B107243A
Fourier transform EPR study and quantum chemical calculations of dihydrofuran radicals formed by triplet sensitized electron transfer in aqueous solution
K. Bernhard, S. Naumov
DOI: 10.1039/B109064J
Kinetics for acid-dissociation of tetraphenylporphinetetrasulfonate in the ground state measured by laser photolysis relaxation method
Satoshi Tsukahara, Hitoshi Watarai
DOI: 10.1039/B108532H
Covalently bound CdTe nanocrystals
Kathrin Hoppe, Ekkehard Geidel, Horst Weller, Alexander Eychmüller
DOI: 10.1039/B201219G
Propagating fronts in periodic precipitation systems with redissolution
DOI: 10.1039/B109278M
Probing the electronic structure of polynuclear metal clusters with total electron spin S > 1/2 and significant zero-field splitting; Application to the clusters of the nitrogenase MoFe-protein
Jan Petersen, David J. Lowe
DOI: 10.1039/B110486C
A hybrid SAM phospholipid approach to fabricating a ‘free’ supported lipid bilayer
Arwel V. Hughes, Arach Goldar, Michael C. Gerstenberg, Steve J. Roser, Jeremy Bradshaw
DOI: 10.1039/B200409G
Oxidation, ignition and combustion of toluene: Experimental and detailed chemical kinetic modeling
P. Dagaut, G. Pengloan, A. Ristori
DOI: 10.1039/B110282F
您可能还喜欢
如何储存8-溴-4-羟基-6-(三氟甲氧基)喹啉-3-羧酸乙酯(CAS号:1072944-81-0)?
8-溴-4-羟基-6-(三氟甲氧基)喹啉-3-羧酸乙酯应储存在阴凉、干燥的地方,避免光照和高温。建议使用密封容器进行储存,以防止水分和空气的影响。
2,2-二(2-呋喃基)丙烷(CAS号:17920-88-6)的市场或研究趋势如何?
2,2-二(2-呋喃基)丙烷的研究趋势主要集中在新型材料的开发和应用,如高分子材料、有机光电材料等。市场趋势方面,随着环保要求的提高和新材料的应用,该化合物的需...
如何处理含有螺[呋喃并[3,4-b]吡啶-5(7H),4'-哌啶]-7-酮盐酸盐(CAS号:475152-31-9)的废料?
对于含有螺[呋喃并[3,4-b]吡啶-5(7H),4'-哌啶]-7-酮盐酸盐的废料,应首先进行分类和分离,以减少危险物质的数量。随后,可以考虑通过化学氧化、生物...
Cinnamyl 3-aminobut-2-enoate(CAS号:113898-97-8)安全吗?
Cinnamyl 3-氨基丁-2-烯酸在接触皮肤和眼睛时可能会引起刺激。应避免吸入其粉尘和烟雾。操作时应穿戴适当的个人防护装备,如手套、护目镜和实验室外套。
反式-2-十二碳烯二酸(CAS号:6402-36-4)的市场或研究趋势如何?
反式-2-十二碳烯二酸在医药、材料科学等领域有一定的应用,但其市场相对较小。近年来,由于环保意识的提升,对环境友好型化学品的需求增加,研究倾向于开发更绿色的合成...
什么是(9ci)-1H-苯并咪唑-5-乙酸(CAS号:473895-86-2)?
(9ci)-1H-苯并咪唑-5-乙酸是一种含氮杂环化合物,其化学结构为1H-苯并咪唑-5-乙酸。该化合物具有特定的分子式C8H7NO2,属于有机酸类化合物。
酞菁蓝(CAS号:147-14-8)的主要用途是什么?
酞菁蓝主要用作颜料和染料,广泛应用于塑料、油墨、涂料、纺织品及橡胶工业中。它也用于光敏材料,如太阳能电池和光刻胶。在医疗领域,酞菁蓝因其光敏特性被用于某些光动力...
5-甲基-1,2,3,4-四氢异喹啉(CAS号:123593-99-7)安全吗?
5-甲基-1,2,3,4-四氢异喹啉在使用和储存时需要谨慎处理。它具有一定的毒性,应避免吸入其蒸气或直接接触皮肤和眼睛。操作此化合物时,建议佩戴防护眼镜、实验服...
如何处理含有3',4',5'-三甲氧基苯乙酮(CAS号:1136-86-3)的废料?
含有3',4',5'-三甲氧基苯乙酮的废液应首先确保其是否为危险废物,根据当地法规确定处理方法。通常,这类有机废液可以采用中和反应降低其pH值,然后通过蒸馏或萃...
如何储存KI-7(CAS号:1489263-00-4)?
KI-7应储存在通风良好的干燥环境中,避免光照和高温。建议使用密封容器储存,并保持在阴凉处。储存温度应控制在室温范围内,一般建议不超过25°C。避免与氧化剂接触...
来源期刊
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.
![2-[(5Z,8Z,11Z,14Z)-5,8,11,14-Icosatetraen-1-yloxy]-1,3-propanediol structure 2-[(5Z,8Z,11Z,14Z)-5,8,11,14-Icosatetraen-1-yloxy]-1,3-propanediol structure](https://cnstatic.chemtradehub.com/structs/222/222723-55-9-0348.webp)
![(4aR,5S,6R,8aS)-5-[2-(3-Furyl)ethyl]-8a-(hydroxymethyl)-5,6-dimethyl-3,4,4a,5,6,7,8,8a-octahydro-1-naphthalenecarboxylic acid structure (4aR,5S,6R,8aS)-5-[2-(3-Furyl)ethyl]-8a-(hydroxymethyl)-5,6-dimethyl-3,4,4a,5,6,7,8,8a-octahydro-1-naphthalenecarboxylic acid structure](https://cnstatic.chemtradehub.com/structs/184/18411-75-1-d4cd.webp)

![N-{3-[Benzyl(methyl)amino]propyl}-9-chloro-5,6,7,8-tetrahydro-2-acridinecarboxamide structure N-{3-[Benzyl(methyl)amino]propyl}-9-chloro-5,6,7,8-tetrahydro-2-acridinecarboxamide structure](https://cnstatic.chemtradehub.com/structs/142/1426944-49-1-1e4c.webp)
![2,4-Dichloro-6-isopropyl-5H-pyrrolo[3,4-d]pyrimidin-7(6H)-one structure 2,4-Dichloro-6-isopropyl-5H-pyrrolo[3,4-d]pyrimidin-7(6H)-one structure](https://cnstatic.chemtradehub.com/structs/107/1079649-94-7-ad4a.webp)