Journal of Raman Spectroscopy
基本信息
The Journal of Raman Spectroscopy is an international journal dedicated to the publication of original research at the cutting edge of all areas of science and technology related to Raman spectroscopy. The journal seeks to be the central forum for documenting the evolution of the broadly-defined field of Raman spectroscopy that includes an increasing number of rapidly developing techniques and an ever-widening array of interdisciplinary applications. Such topics include time-resolved, coherent and non-linear Raman spectroscopies, nanostructure-based surface-enhanced and tip-enhanced Raman spectroscopies of molecules, resonance Raman to investigate the structure-function relationships and dynamics of biological molecules, linear and nonlinear Raman imaging and microscopy, biomedical applications of Raman, theoretical formalism and advances in quantum computational methodology of all forms of Raman scattering, Raman spectroscopy in archaeology and art, advances in remote Raman sensing and industrial applications, and Raman optical activity of all classes of chiral molecules.
CiteScore
| 学科 | 排名 | 百分位 |
|---|---|---|
Materials ScienceGeneral Materials Science |
166 / 463 | 64% |
期刊统计
投稿信息
投稿网址:
http://mc.manuscriptcentral.com/jrs相关文献
Origin of surface trap states in CdS quantum dots: relationship between size dependent photoluminescence and sulfur vacancy trap states
Aisea Veamatahau, Bo Jiang, Tom Seifert, Satoshi Makuta, Kay Latham, Masayuki Kanehara, Toshiharu Teranishi
DOI: 10.1039/C4CP04761C
Influence of dispersive forces on the final shape of a reverse micelle
I. León, R. Montero, A. Longarte, José A. Fernández
DOI: 10.1039/C4CP03667K
Bimodal crystallization at polymer–fullerene interfaces
Dyfrig Môn, Anthony M. Higgins, David James, Mark Hampton, J. Emyr Macdonald, Michael B. Ward, Philipp Gutfreund, Samuele Lilliu, Jonathan Rawle
DOI: 10.1039/C4CP04253K
Ligand(s)-to-metal charge transfer as a factor controlling the equilibrium constants of late first-row transition metal complexes: revealing the Irving–Williams thermodynamical series
Pradeep R. Varadwaj, Arpita Varadwaj, Bih-Yaw Jin
DOI: 10.1039/C4CP03953J
Chemical imaging of single catalyst particles with scanning μ-XANES-CT and μ-XRF-CT
S. W. T. Price, K. Ignatyev, K. Geraki, M. Basham, J. Filik, N. T. Vo, P. T. Witte, J. F. W. Mosselmans
DOI: 10.1039/C4CP04488F
Optimal top electrodes for inverted polymer solar cells
Hye Rim Yeom, Jungwoo Heo, Gi-Hwan Kim, Seo-Jin Ko, Seyeong Song, Yimhyun Jo, Dong Suk Kim, Bright Walker, Jin Young Kim
DOI: 10.1039/C4CP04788E
Ab initio quantum dynamical analysis of ultrafast nonradiative transitions via conical intersections in pyrazine
Manabu Kanno, Yuta Ito, Noriyuki Shimakura, Shiro Koseki, Hirohiko Kono
DOI: 10.1039/C4CP04807E
The photochemistry of inverse dithienylethene switches understood
Stéphane Aloïse, Ruan Yibin, Ismail Hamdi, Guy Buntinx, Aurélie Perrier, François Maurel, Denis Jacquemin, Michinori Takeshita
DOI: 10.1039/C4CP03641G
Formation of 2- and 1-methyl-1,4-dihydronaphthalene isomers via the crossed beam reactions of phenyl radicals (C6H5) with isoprene (CH2C(CH3)CHCH2) and 1,3-pentadiene (CH2CHCHCHCH3)
Tao Yang, Lloyd Muzangwa, Dorian S. N. Parker, Ralf I. Kaiser, Alexander M. Mebel
DOI: 10.1039/C4CP04612A
Dirac fermions in silicene on Pb(111) surface
Agata Podsiadły-Paszkowska, Mariusz Krawiec
DOI: 10.1039/C4CP05104A
您可能还喜欢
4-[4-三氟甲基苯基]恶唑(CAS号:1126636-40-5)通常如何合成?
4-[4-三氟甲基苯基]恶唑通常通过将4-三氟甲基苯酚与异硫氰酸苯酯在有机溶剂中进行酯化反应合成。该反应可在无水条件下,使用适当的催化剂,如四丁基氢氧化铵,以提...
RockPhos Pd G3(CAS号:2009020-38-4)通常如何合成?
RockPhos Pd G3 通常通过钯催化偶联反应合成,使用配体 (2'-Amino-2-biphenylyl)(methanesulfonato-kappa...
1-哌啶甲酰胺(CAS号:2158-03-4)的市场或研究趋势如何?
1-哌啶甲酰胺作为有机合成中的重要中间体,其市场需求主要受医药、农药、染料等行业推动。近年来,随着新药开发和绿色化学的发展,该化合物的研究趋势集中在开发更高效、...
2-(二苯基膦基)乙胺(CAS号:4848-43-5)适用哪些法规指南?
2-(二苯基膦基)乙胺适用于多种法规指南,包括但不限于《全球化学品统一分类和标签制度》(GHS),欧盟《化学品注册、评估、授权和限制》法规(REACH),以及美...
如何储存间苯二甲酸二烯丙酯(CAS号:1087-21-4)?
间苯二甲酸二烯丙酯应储存在阴凉、干燥、通风良好的地方,远离火源和热源。储存容器应密封,避免光照和高温。储存温度应控制在25℃以下,相对湿度应低于80%。避免与其...
什么是间甲苯异硫代异氰酸酯(CAS号:621-30-7)?
间甲苯异硫代异氰酸酯是一种有机化合物,分子式为C7H7NO2S,具有刺激性气味。它是一种重要的有机合成中间体,在合成其他化合物时广泛应用。
在合成中是否有N-Boc-D-苯丙氨醇(CAS号:106454-69-7)的替代品?
在合成中,可以考虑使用N-Cbz-D-苯丙氨醇或N-Fmoc-D-苯丙氨醇作为替代品。这些化合物同样具有保护氨基的功能,且在合成过程中表现出良好的反应性能。
3-羟甲基-2-氧异丙基吡啶(CAS号:954240-50-7)的主要用途是什么?
3-羟甲基-2-氧异丙基吡啶主要用于有机合成领域,可以作为合成其他药物、农药或精细化学品的中间体。此外,它还可能在实验室研究中作为特定反应的前体或溶剂。
6-氨基-9-甲基嘌呤(CAS号:700-00-5)应用于哪些行业?
6-氨基-9-甲基嘌呤目前主要应用于医药行业,作为某些药物的中间体。此外,它还可能用于聚合物、传感器和半导体的某些领域,作为功能性单体或掺杂剂。










![1-(Hexopyranosyloxy)-4a,5-dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl 3-phenylacrylate structure 1-(Hexopyranosyloxy)-4a,5-dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl 3-phenylacrylate structure](https://cnstatic.chemtradehub.com/structs/192/19210-12-9-ecae.webp)




![2-Bromodibenzo[b,d]furan structure 2-Bromodibenzo[b,d]furan structure](https://cnstatic.chemtradehub.com/structs/86-/86-76-0-1814.webp)

