Non-linear photoelectron effect contributes to the formation of negative matrix ions in UV-MALDI
文献情報
E. Alonso, R. Zenobi
The mechanism of negative ion formation in matrix-assisted laser desorption/ionization (MALDI) is less well understood than that of positive ions: electron capture, disproportionation, and liberation of negatively charged sample molecules or clusters have been proposed to produce the initial anions in MALDI. Here, we propose that the non-linear photoelectric effect can explain the emission of electrons from the metallic target material. Moreover, electrons with sufficient kinetic energy (0–10 eV) could be responsible for the formation of initial negative ions. Gas-phase electron capture by neutral 2,5-dihydroxy benzoic acid (DHB) to yield M− is investigated on the basis of a coupled physical and chemical dynamics (CPCD) theory from the literature. A three-layer energy mass balance model is utilized to calculate the surface temperature of the matrix, which is used to determine the translational temperature, the number of desorbed matrix molecules per unit area, and the ion velocity. Calculations of dissociative attachment and autoionization rates of DHB are presented. It was found that both processes contribute significantly to the formation of [M − H]− and [M − H2]−, although the predicted yield in the fluence range of 5−100 mJ cm−2 is low, certainly less than that for positive ions M+. This work represents the first proposal for a comprehensive theoretical description of negative ion formation in UV-MALDI.
関連文献
First successful application of diphosphite ligands in the asymmetric hydroformylation of dihydrofurans
Montserrat Diéguez, Oscar Pamies, Carmen Claver
DOI: 10.1039/B416514D
Monitoring the effect of ultrafast deactivation of the electronic excited states of DNA bases and polynucleotides following 267 nm laser excitation using picosecond time-resolved infrared spectroscopy
Marina K. Kuimova, Joanne Dyer, Michael W. George, David C. Grills, John M. Kelly, Pavel Matousek, Anthony W. Parker, Xue Zhong Sun, Michael Towrie, Aine M. Whelan
DOI: 10.1039/B414450C
Using ring strain to inhibit a decomposition path: first synthesis of an Alkyl-BIAN ligand (Alkyl-BIAN = bis(alkyl)acenaphthenequinonediimine)
Fabio Ragaini, Michela Gasperini, Emma Gallo, Piero Macchi
DOI: 10.1039/B415767B
Enantioselective chlorination and fluorination of β-keto phosphonates catalyzed by chiral Lewis acids
Luca Bernardi, Karl Anker Jørgensen
DOI: 10.1039/B415568H
Synthesis and crystal structure of the first lanthanide complex of N-confused porphyrin with an η2 agostic C–H interaction
Xunjin Zhu, Wai-Kwok Wong, Wing-Kit Lo, Wai-Yeung Wong
DOI: 10.1039/B415609A
Acoustic coupling at multiple interfaces and the liquid phase response of the thickness shear-mode acoustic wave sensor
Jonathan S. Ellis, Michael Thompson
DOI: 10.1039/B402822H
A one-dimensional array with controlled length from a PYBOX dimer with flexible oligo(sec-dialkylammonium cations)
Takahiro Sugimoto, Kazuki Sada, Shigeru Sakamoto, Kentaro Yamaguchi, Seiji Shinkai
DOI: 10.1039/B316204D
Efficient protein–ligand interaction by guaranteeing mesospacing between immobilized biotins
Young-Seo Choi, Chang Won Yoon, Hae Dong Lee, Minyoung Park, Joon Won Park
DOI: 10.1039/B403797A
Exploiting phenyl embraces and π-stacking in the assembly of arrays of tetraphenylphosphonium p-sulfonatocalix[4]arene
Mohamed Makha, Colin L. Raston, Alexandre N. Sobolev, Allan H. White
DOI: 10.1039/B402327G
こちらもおすすめ
2-メトキシ-4-(メチルスルフィニル)アミンの主な用途は何ですか?
2-メトキシ-4-(メチルスルフィニル)アミンは、主に医薬品および農薬の製造に使用されます。また、合成化学の一部として研究用材料としても利用されます。
4,6-二氯-N-甲基ピラミジンアミンの代替品はありますか?
代替品としては、4,6-二クロロピラミジンアミンや他のピラミジン系化合物が考えられます。ただし、目的と用途によって最適な代替品は異なります。
6-氯-4-甲基-1H-吲哚を含む廃棄物はどのように処理すべきですか?
6-氯-4-甲基-1H-吲哚の廃棄物は、適切な容器に収集し、密閉して保管します。温度は常温、湿度は低く、直射日光を避けて保管することを推奨します。廃棄処理は専門...
2-フローユロ-4-(トリフルオロメチル)ベンゾイドについて「に適用される法規ガイドラインは何ですか」
2-フローユロ-4-(トリフルオロメチル)ベンゾイドのCAS番号は207974-08-1です。この化合物はGHS分類で毒性物質と有害な反応物質として分類されます...
4-ニトロフェニルN-[(ベンゼルオキシルカーボンイル]グリシングリシングリシン酸はどのように保存すればよいですか?
4-ニトロフェニルN-[(ベンゼルオキシルカーボンイル]グリシングリシングリシン酸は、室温で暗所に保管し、乾燥した環境で保存することを推奨します。容器は密閉性の...
イソデスロラタドリンの代替品はありますか?
イソデスロラタドリンの代替品としては、デスロラタドリンや他の抗ヒスタミン薬が挙げられます。具体的には、デスロラタドリン、ラセカミド、フェルタドリンなどが、症状や...
5-甲氧基-1,2,3,4-四氢异喹啉盐酸盐はどのように合成されますか?
5-甲氧基-1,2,3,4-四氢异喹啉盐酸盐の一般的な合成方法は、メタノール中で5-メトキシ-1,2,3,4-四ヒュドロイソキシンを塩酸で塩化します。この反応で...
4-アミノ-5-メトキシ-2-トルエンサルホニック酸についての法規ガイドラインは何ですか?
CAS番号6471-78-9の4-アミノ-5-メトキシ-2-トルエンサルホニック酸は、GHS分類では corrosive(腐食性)と識別されます。EUのREAC...
甲基孕酮を取り扱う際の実験室安全事項は何ですか?
甲基孕酮の取り扱いは、PPE(個人保護具)の使用が必要な重要な安全事項を伴います。防塵マスク、ゴーグル、手袋を着用することが推奨されます。ドラフトチャンバーを使...
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.













![tert-Butyl 6-chloro-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylate structure tert-Butyl 6-chloro-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylate structure](https://static.chemtradehub.com/structs/101/1011482-37-3-88a5.webp)
![[5-fluoro-2-(morpholine-4-carbonyl)phenyl]boronic acid structure [5-fluoro-2-(morpholine-4-carbonyl)phenyl]boronic acid structure](https://static.chemtradehub.com/structs/121/1217501-26-2-505c.webp)