Quantum-classical dynamics of the capture of neon atoms by superfluid helium nanodroplets
文献情報
Miquel Blancafort-Jorquera, Arnau Vilà, Miguel González
The capture of a Ne atom by a superfluid helium nanodroplet, Ne + (4He)N → Ne@(4He)N′ + (N − N′) 4He, was studied using a hybrid quantum (helium)–classical (Ne) approach and taking into account the angular momentum. The atom is captured by (4He)N and follows elliptical rotating trajectories, and large energy and angular momentum transfer from the atom to the nanodroplet occur. Evaporation of helium atoms from (4He)N allows removal of the excess energy and angular momentum of the doped nanodroplet. The behaviours observed for angular momentum different from zero are similar to the zero angular momentum case. The angular momentum of the Ne atom can induce vortex nucleation for high enough initial angular momentum values (∼176.3–220.3 ℏ). Vortices arise from collapse of the surface excitations (ripplons) and are long-lived under some initial conditions. Comparison with our own previous quantum dynamics study at zero angular momentum shows that quantum effects are not important under the initial conditions examined here. Besides, a comparison with the scarce information available on other systems has been performed, showing the rich variety of behaviours that can be observed in the solvation of impurities by superfluid helium. More efforts are welcome in order to obtain a deeper insight into the dynamics of the capture process, especially in the vortex formation context.
おすすめジャーナル

Russian Journal of Applied Chemistry

Drug Discovery Today

Organic Process Research & Development

Current Opinion in Colloid & Interface Science

Saudi Pharmaceutical Journal

Journal of Peptide Science

Chemistry Education Research and Practice

New Journal of Chemistry

Acta Materialia

Russian Journal of Coordination Chemistry
関連文献
An “active” and self-switchable nanoreactor
Bo Peng, Xinhua Yuan, Maiyong Zhu, Songjun Li
DOI: 10.1039/C3PY01074K
Polymerizable aggregation-induced emission dye-based fluorescent nanoparticles for cell imaging applications
Xiqi Zhang, Bin Yang, Meiying Liu, Wanyun Liu, Yiwang Chen, Yen Wei
DOI: 10.1039/C3PY01226C
Chalcone derivatives as highly versatile photoinitiators for radical, cationic, thiol–ene and IPN polymerization reactions upon exposure to visible light
Mohamad-Ali Tehfe, Frédéric Dumur, Pu Xiao, Marie Delgove, Bernadette Graff, Jean-Pierre Fouassier, Didier Gigmes, Jacques Lalevée
DOI: 10.1039/C3PY00922J
Sulfonated poly(arylene ether phosphine oxide)s with various distributions and contents of pendant sulfonic acid groups synthesized by direct polycondensation
Huiying Liao, Ke Zhang, Gangsheng Tong, Guyu Xiao, Deyue Yan
DOI: 10.1039/C3PY00821E
Synthesis of well-defined amphiphilic branched polyethylene-graft-poly (N-isopropylacrylamide) copolymers by coordination copolymerization in tandem with RAFT polymerization and their self-assembled vesicles
Ye Zhao, Haiyang Gao, Guodong Liang, Fangming Zhu, Qing Wu
DOI: 10.1039/C3PY01289A
Porphyrin-containing hyperbranched supramolecular polymers: enhancing 1O2-generation efficiency by supramolecular polymerization
Yiliu Liu, Zehuan Huang, Kai Liu, Hans Kelgtermans, Wim Dehaen, Zhiqiang Wang, Xi Zhang
DOI: 10.1039/C3PY01036H
The relationship between the degree of branching and glass transition temperature of branched polyethylene: experiment and simulation
Xiang Luo, Shijie Xie, Jun Liu, Haibin Hu, Jing Jiang, Wei Huang, Haiyang Gao, Dongshan Zhou, Zhongyuan Lü, Deyue Yan
DOI: 10.1039/C3PY00896G
Synthesis and evaluation of thermally-responsive coatings based upon Diels–Alder chemistry and renewable materials
Dahlia N. Amato, Gregory A. Strange, John P. Swanson, Anton D. Chavez, Suzanne E. Roy, Kim L. Varney, Craig A. Machado, Douglas V. Amato, Philip J. Costanzo
DOI: 10.1039/C3PY01024D
Neutral linear amphiphilic homopolymers prepared by atom transfer radical polymerization
Yi Wang, Alina M. Alb, Jibao He, Scott M. Grayson
DOI: 10.1039/C3PY00916E
こちらもおすすめ
「邻羟基阿托伐他汀内酯标准品」に適用される法規ガイドelinesは何ですか?
CAS番号163217-74-1の「邻羟基阿托伐他汀内酯标准品」は、GHS分類では危険物に分類されず、主にREACH規則とFDA/EPAの管理対象となります。R...
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩の主な用途は何ですか?
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩は、医薬品や合成化学の研究に広く用いられます。また、特定の薬物の前...
トランス-4-メチルピロリジン-3-オール塩酸塩はどのように合成されますか?
トランス-4-メチルピロリジン-3-オール塩酸塩は、4-メチルピロリジンの塩酸塩化によって合成されます。一般的な合成方法では、4-メチルピロリジンを塩酸に加えて...
硫雜環丁烷-1,1-二氧化物は安全ですか?
硫雜環丁烷-1,1-二氧化物は安全ではありません。毒性は報告されていませんが、高温下で分解し、可燃性があるため、高圧ガスは注意が必要です。密閉した容器で保管し、...
9-ヒドロキシエリプチシネ塩酸塩はどのように合成されますか?
9-ヒドロキシエリプチシネ塩酸塩は、エリプチシネから塩酸を添加することで合成されます。選択性は高いですが、収率は約70%です。
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮の物理化学的性質は何ですか?
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮のCAS番号は5621-86-3です。この化合物は白色の結晶性粉末で、分子量は415.03で...
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪はどのように保存すればよいですか?
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪は、直射日光を避けて暗所に、室温(15-25℃)で保管し、密閉容器に入れることで安定性を保つことができます。
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンの主な用途は何ですか?
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンは、医薬品の合成、有機合成化学、および新材料の研究で使用され...
掲載誌
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.



![[(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-Diacetyloxy-15-[(2R,3S)-3-benzamido-3-phenyl-2-(2,2,2-trichloroethoxycarbonyloxy)propanoyl]oxy-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate structure [(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-Diacetyloxy-15-[(2R,3S)-3-benzamido-3-phenyl-2-(2,2,2-trichloroethoxycarbonyloxy)propanoyl]oxy-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate structure](https://static.chemtradehub.com/structs/100/100431-55-8-7104.webp)
