Study of the CH3⋯H2O radical complex stabilized in helium nanodroplets
文献情報
Svemir Rudić, Jeremy M. Merritt, Roger E. Miller
The weakly bound CH3⋯H2O radical complex has been investigated by infrared laser spectroscopy. The complex is stabilized in helium nanodroplets and prepared by sequential pick up of a methyl radical and water molecule. Partially rotationally resolved spectra corresponding to the v = 1 ← 0 excitation of the symmetric H2O stretching vibration within the complex show a significant red shift (25.06 cm−1) when compared with the symmetric stretch of H2O monomer, in agreement with the hydrogen bonded like structure derived by theory. Additional broad features were observed in the region predicted by theory for the antisymmetric stretch supporting our assignment. The B rotational constant is found to be 3.03 times smaller than predicted by ab initio calculations, with the reduction being attributed to the effects of helium solvation. The permanent electric dipole moment of the complex is experimentally determined to be 2.1 ± 0.3 D using Stark spectroscopy. Ab initio calculations are also reported that provide support to the experimental results, as well as investigate the nature of large amplitude vibrational motion within the complex.
関連文献
Stereoselective synthetic strategies of stereogenic carbon centers featuring a difluoromethyl group
Fengyun Gao, Boyu Li, Yalan Wang, Qushuo Chen, Yongzhen Li, Kairong Wang, Wenjin Yan
DOI: 10.1039/D1QO00032B
Improved synthesis of symmetrically & asymmetrically N-substituted pyridinophane derivatives
Andrew J. Wessel, Jason W. Schultz, Fengzhi Tang, Hui Duan, Liviu M. Mirica
DOI: 10.1039/C7OB02508D
Pd-Catalyzed one-pot sequential cross-coupling reactions of tetrabromothiophene
Kapil Mohan Saini, Rakesh K. Saunthwal, Akhilesh K. Verma
DOI: 10.1039/C7OB02601C
XtalFluor-E® mediated proto-functionalization of N-vinyl amides: access to N-acetyl N,O-acetals
Y. Yi, H. Gholami, M. G. Morrow, B. Borhan
DOI: 10.1039/C7OB02283B
Recent advances in sustainable synthesis of N-heterocycles following acceptorless dehydrogenative coupling protocol using alcohols
Milan Maji, Dibyajyoti Panja, Ishani Borthakur, Sabuj Kundu
DOI: 10.1039/D0QO01577F
Water-soluble and UV traceable isatoic anhydride-based reagents for bioconjugation
Adam Fessler, Corey Garmon, Thomas Heavey, Anthony Fowler, Craig Ogle
DOI: 10.1039/C7OB02377D
Design and self-assembly of PBLG-b-ELP hybrid diblock copolymers based on synthetic and elastin-like polypeptides
Jean-Michel Guigner
DOI: 10.1039/C7OB01945A
Synthesis and photophysical properties of donor-substituted phenyl-phosphachromones as potential TADF materials
Shuangshuang Xu, Haiyang Huang, Chengxiong Yuan, Fen Liu, Haixin Ding, Qiang Xiao
DOI: 10.1039/D1QO00121C
こちらもおすすめ
2-氟-4-イオドベンzo酸エチルエステルを取り扱う際の実験室安全事項は何ですか?
2-氟-4-イオドベンzo酸エチルエステルは有機溶媒を用いた反応であり、ドラフトチャンバーでの操作が必要です。漏洩時にはSDS参照の安全措置を講じ、PPE(防護...
血根碱の主な用途は何ですか?
血根碱は主に医薬分野で利用され、抗炎症や抗がん剤としての潜在的な効果が研究されています。また、化学研究や薬物開発において、新しい薬剤設計の参考となる化合物として...
Methyl 3-methoxythiophene-2-carboxylateの主な用途は何ですか?
Methyl 3-メトキシスチフェン-2-カルボン酸メチルエステルは、薬品合成、染料製造、以及合成中間体としての用途が広がっています。
丹磺酰-L-亮氨酸はどのように保存すればよいですか?
丹磺酰-L-亮氨酸は乾燥した場所で、直射日光から保護し、低温(室温以下)で保存してください。密閉容器に入れて保管することをおすすめします。
5-(苄氧基)ピラミジン-4-アミンの代替品はありますか?
5-(苄氧基)ピラミジン-4-アミンの代替品として、6-メトキシピラミジンや5-フェニルピラミジンなどが挙げられます。これらの化合物は、5-(苄氧基)ピラミジン...
8-ヒドロキシノルデコペントアセートの物理化学的性質は何ですか?
8-ヒドロキシノルデコペントアセートはCAS番号84807-87-4の化合物で、分子量は750.02 uです。これは油溶性で、水に溶けにくい特徴があります。反応...
tert-ブチル(エス)-1-ヒドロキシペンタ-4-エン-2-イルカルバamateの主な用途は何ですか?
tert-ブチル(エス)-1-ヒドロキシペンタ-4-エン-2-イルカルバamateは主に医薬品の合成材料や分析化学の試薬として使用されます。
ブコール-L-2-フローヨルブリンについて適切な法規ガイドラインは何ですか?
ブコール-L-2-フローヨルブリン(CAS番号: 1196107-73-9)は、GHS(グローバルハザードアサessmentシステム)に基づく危害分類と表示が求...
6-ブロモ-N-環丙基-2-ピリジニニメタンの市場動向や研究トレンドはどうですか
6-ブロモ-N-環丙基-2-ピリジニニメタンは、薬理学研究や合成化学に使用される化合物であり、特に抗ウイルス薬や抗がん薬の開発に注目されています。市場では、薬物...
RS-AMPÀはどのように保存すればよいですか?
RS-AMPÀは、遮光容器に保存し、室温(15〜25℃)で保管することが推奨されます。高湿や熱は物質を劣化させるため、湿度は50%以下に保つことが重要です。また...
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.













![4-[2-(Trichlorosilyl)ethyl]benzenesulfonyl chloride structure 4-[2-(Trichlorosilyl)ethyl]benzenesulfonyl chloride structure](https://static.chemtradehub.com/structs/797/79793-00-3-de16.webp)
