Reversible ferromagnetic–antiferromagnetic transformation upon dehydration–hydration of the nanoporous coordination framework, [Co3(OH)2(C4O4)2]·3H2O
文献信息
Mohamedally Kurmoo, Hitoshi Kumagai, Karena W. Chapman, Cameron J. Kepert
Reversible crystal-to-crystal transformation accompanied by change from ferromagnetic to antiferromagnetic ground states at 8 K upon dehydration–rehydration of the nanoporous coordination framework [CoII3(OH)2(C4O4)2]·3H2O.
相关文献
Cyclopropanation of alkenes with metallocarbenes generated from monocarbonyl iodonium ylides
Tristan Chidley, Graham K. Murphy
DOI: 10.1039/C8OB02636J
The type I rat fatty acid synthase ACP shows structural homology and analogous biochemical properties to type II ACPs
Michelle A. C. Reed, Michael Schweizer, Anna E. Szafranska, Chris Arthur, Thomas P. Nicholson, Russell J. Cox, John Crosby, Matthew P. Crump, Thomas J. Simpson
DOI: 10.1039/B208941F
Syntheses and anti-cancer activity of CO-releasing molecules with targeting galactose receptors
Jili Li, Jinlong Zhang, Qiuping Zhang, Zhongjie Bai, Quanyi Zhao, Dian He, Zhen Wang, Yonglin Chen, Bin Liu
DOI: 10.1039/C8OB01921E
Novel 3-phenylprop-2-ynylamines as inhibitors of mammalian squalene epoxidase
David L. Musso, Morris J. Clarke, James L. Kelley, G. Evan Boswell, Grace Chen
DOI: 10.1039/B209165H
Investigations into the mechanism of action of nitrobenzene as a mild dehydrogenating agent under acid-catalysed conditions
M. Lurdes S. Cristiano, David J. P. Gago, Antonio M. d'A. Rocha Gonsalves, Robert A. W. Johnstone, Moya McCarron
DOI: 10.1039/B210887A
Synthesis, absolute configuration and conformation of optically active 1,2-homoheptafulvalene
Shunji Ito, Mitsuhiro Kurita, Sigeru Kikuchi, Toyonobu Asao, Yoshitora Ito, Masaji Oda, Hideo Sotokawa, Akio Tajiri, Noboru Morita
DOI: 10.1039/B210949M
New strategies and building blocks for functionalised 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene derivatives, including pyrrolo-annelated derivatives and π-extended systems with intramolecular charge-transfer‡
Christian A. Christensen, Martin R. Bryce, Andrei S. Batsanov, Jan Becher
DOI: 10.1039/B211153P
Preparation and use as spin trapping agents of new ester-nitrones
Ahmad Allouch, Valérie Roubaud, Robert Lauricella, Jean-Claude Bouteiller, Béatrice Tuccio
DOI: 10.1039/B210035E
Studies of 4-arylthiazolylhydrazones derived from 1-indanones as Trypanosoma cruzi squalene epoxidase inhibitors by molecular simulations
Lucas E. Fabian
DOI: 10.1039/C8OB02310G
The selective functionalisation and difunctionalisation of p-substituted calix[6]arene and calix[8]arenes using hydrophilic moieties
Gwénaëlle Hervé, Dirk Uwe Hahn, Anne-Cécile Hervé, Kerry J. Goodworth, Alison M. Hill, Helen C. Hailes
DOI: 10.1039/B208649M
您可能还喜欢
N-2,2-丙烯基-2-丙烯酰胺(CAS号:2555-13-7)通常如何合成?
N-2,2-丙烯基-2-丙烯酰胺通常通过丙烯酰胺与丙烯基卤化物的缩合反应合成。该反应通常在温和的条件下进行,使用适量的碱如吡啶作为催化剂。反应的选择性良好,产率...
什么是1,2-二碘四氟代乙烷(CAS号:354-65-4)?
1,2-二碘四氟代乙烷是一种有机化合物,化学式为C2F4I2,CAS号为354-65-4。它是一种无色透明液体,具有特殊的化学性质和物理性质,包括高沸点、低挥发...
3-溴-1H-吡咯[3,2-c]吡啶-4-碳腈(CAS号:1000341-71-8)适用哪些法规指南?
根据GHS(全球化学品统一分类和标签制度),3-溴-1H-吡咯[3,2-c]吡啶-4-碳腈被归类为第2类易燃液体。在欧盟,该化合物需要符合REACH法规的要求,...
1-氯甲基萘磺酸(CAS号:87491-79-0)安全吗?
1-氯甲基萘磺酸在使用时需要谨慎,因为它具有一定的刺激性和腐蚀性。操作时应佩戴适当的防护装备,如防化服、手套、护目镜等,避免直接接触皮肤和吸入其蒸汽。
二氯(二环戊二烯)铂(CAS号:12083-92-0)的主要用途是什么?
该化合物主要用于催化剂领域,特别是在有机合成中的催化氧化反应以及作为某些药物合成的中间体。此外,它还被研究用于纳米材料的制备。
3-溴-7-氯噻吩并[3,2-b]吡啶-6-甲腈(CAS号:798574-82-0)安全吗?
3-溴-7-氯噻吩并[3,2-b]吡啶-6-甲腈在处理时需要谨慎,因其含有溴和氯等强卤素,可能具有一定的刺激性和腐蚀性。使用时应佩戴适当的个人防护装备,避免皮肤...
(R)-1-((R)-2-(2’-二环己基膦苯基)三戊铁基]乙基(双-3,5-三氟甲基苯基)膦(CAS号:494227-32-6)的主要用途是什么?
该化合物主要用于有机合成领域,特别是作为催化剂或配体,在有机合成反应中发挥重要作用。此外,它还可能应用于催化加氢反应、偶联反应等。
3-[6-(Diphenylphosphoryl)-2-naphthyl]-1,10-phenanthroline(CAS号:1480371-38-7)安全吗?
3-[6-(Diphenylphosphoryl)-2-naphthyl]-1,10-phenanthroline在正常使用条件下相对安全,但在操作时应穿戴适当...
在合成中是否有ETHYL 2-(4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)CYCLOHEX-3-ENYL)ACETATE(CAS号:1166829-70-4)的替代品?
可以考虑使用类似结构的化合物作为替代品,如2-(4-环戊基环己烯基)乙酸酯,这种化合物在结构上相似,可能在某些合成路径中作为替代品。
如何处理含有3-(3-氨基丙基)丙酮缩甘油(CAS号:131606-42-3)的废料?
处理含有3-(3-氨基丙基)丙酮缩甘油的废料时,首先应确保遵守当地的环保法规。对于危险废物,应进行分类收集,然后送至专业的废物处理设施进行焚烧或安全填埋。在处理...
来源期刊
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry










![1H-Imidazo[4,5-c]pyridine-7-carboxylic acid structure 1H-Imidazo[4,5-c]pyridine-7-carboxylic acid structure](https://cnstatic.chemtradehub.com/structs/123/1234616-39-7-1344.webp)

![(1R,6R)-6-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-cyclohexene-1-carboxylic acid structure (1R,6R)-6-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-cyclohexene-1-carboxylic acid structure](https://cnstatic.chemtradehub.com/structs/865/865689-24-3-5fef.webp)

