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Journal articles on the topic 'Carbon chemistry'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Li, Xiaoxian, Tongxing Liu, Beibei Zhang, et al. "Formation of Carbon-Carbon Bonds Mediated by Hypervalent Iodine Reagents Under Metal-free Conditions." Current Organic Chemistry 24, no. 1 (2020): 74–103. http://dx.doi.org/10.2174/1385272824666200211093103.

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During the past several decades, hypervalent iodine reagents have been widely used in various organic transformations. Specifically, these exclusive classes of reagents have been extensively used for the construction of carbon-carbon bonds. This review aims to cover all the reactions involving the construction of carbon-carbon bonds mediated by hypervalent iodine reagents, providing references and highlights for synthetic chemists who are interested in hypervalent iodine chemistry.

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2

Langer, W. D. "Carbon Isotopic Chemistry." Symposium - International Astronomical Union 150 (1992): 193–97. http://dx.doi.org/10.1017/s0074180900090008.

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Isotopic molecular abundances are used to interpret Galactic chemical evolution and the properties of interstellar clouds. The isotopic chemistry of carbon plays an important role in the interpretation of these measurements. This paper reviews the recent measurements of the carbon twelve to thirteen ratio across the Galaxy and the isotopic chemistry.

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3

Olchowski, Rafał, Emil Zięba, Dimitrios A. Giannakoudakis, Ioannis Anastopoulos, Ryszard Dobrowolski, and Mariusz Barczak. "Tailoring Surface Chemistry of Sugar-Derived Ordered Mesoporous Carbons towards Efficient Removal of Diclofenac from Aquatic Environments." Materials 13, no. 7 (2020): 1625. http://dx.doi.org/10.3390/ma13071625.

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Ordered mesoporous carbon (CMK-3), obtained from an abundant natural source, sugar, was thermochemically modified with dicyandiamide and thiourea as well as by classical oxidization with hydrogen peroxide to introduce specific surface groups. Thermochemical modifications resulted in carbon with almost unchanged porosity and altered surface chemistry while porosity of H2O2-treated carbon was seriously deteriorated. The obtained carbons were tested as sorbents of diclofenac, considered as one of the emerging water contaminants. Changes in porosity and surface chemistry of modified carbons result

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4

Chen, Xiang, Xiao-Ru Chen, Ting-Zheng Hou, et al. "Lithiophilicity chemistry of heteroatom-doped carbon to guide uniform lithium nucleation in lithium metal anodes." Science Advances 5, no. 2 (2019): eaau7728. http://dx.doi.org/10.1126/sciadv.aau7728.

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The uncontrollable growth of lithium (Li) dendrites seriously impedes practical applications of Li metal batteries. Various lithiophilic conductive frameworks, especially carbon hosts, are used to guide uniform Li nucleation and thus deliver a dendrite-free composite anode. However, the lithiophilic nature of these carbon hosts is poorly understood. Herein, the lithiophilicity chemistry of heteroatom-doped carbon is investigated through both first principles calculations and experimental verifications to guide uniform Li nucleation. The electronegativity, local dipole, and charge transfer are

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5

Lin, Tong, Vardhan Bajpai, Tao Ji, and Liming Dai. "Chemistry of Carbon Nanotubes." Australian Journal of Chemistry 56, no. 7 (2003): 635. http://dx.doi.org/10.1071/ch02254.

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Judicious application of site-selective reactions to non-aligned and aligned carbon nanotubes has opened a rich field of carbon nanotube chemistry. In order to meet specific requirements demanded by particular applications (e.g. biocompatibility for nanotube biosensors and interfacial strength for blending with polymers), chemical modification of carbon nanotubes is essential. The tips of carbon nanotubes are more reactive than their sidewalls, allowing a variety of chemical reagents to be attached at the nanotube tips. Recently, some interesting reactions have also been devised for chemical m

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6

Oliva-Enrich, Josep M., Ibon Alkorta, and José Elguero. "Hybrid Boron-Carbon Chemistry." Molecules 25, no. 21 (2020): 5026. http://dx.doi.org/10.3390/molecules25215026.

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The recently proved one-to-one structural equivalence between a conjugated hydrocarbon CnHm and the corresponding borane BnHm+n is applied here to hybrid systems, where each C=C double bond in the hydrocarbon is consecutively substituted by planar B(H2)B moieties from diborane(6). Quantum chemical computations with the B3LYP/cc-pVTZ method show that the structural equivalences are maintained along the substitutions, even for non-planar systems. We use as benchmark aromatic and antiaromatic (poly)cyclic conjugated hydrocarbons: cyclobutadiene, benzene, cyclooctatetraene, pentalene, benzocyclobu

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7

Tasis, Dimitrios, Nikos Tagmatarchis, Alberto Bianco, and Maurizio Prato. "Chemistry of Carbon Nanotubes." Chemical Reviews 106, no. 3 (2006): 1105–36. http://dx.doi.org/10.1021/cr050569o.

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8

Sakai, Nami, and Satoshi Yamamoto. "Warm Carbon-Chain Chemistry." Chemical Reviews 113, no. 12 (2013): 8981–9015. http://dx.doi.org/10.1021/cr4001308.

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9

Alcarazo, Manuel, Christian W. Lehmann, Anakuthil Anoop, Walter Thiel, and Alois Fürstner. "Coordination chemistry at carbon." Nature Chemistry 1, no. 4 (2009): 295–301. http://dx.doi.org/10.1038/nchem.248.

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10

Uppenbrink, J. "CHEMISTRY: Carbon Chain Gangs." Science 287, no. 5457 (2000): 1365c—1365. http://dx.doi.org/10.1126/science.287.5457.1365c.

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11

Jampilek, Josef. "Heterocycles in Medicinal Chemistry." Molecules 24, no. 21 (2019): 3839. http://dx.doi.org/10.3390/molecules24213839.

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Heteroatoms constitute a very common fragment of a number of active pharmaceutical ingredients as well as excipients; from the point of view of significance, it is all the same if these are isosterically/bioisosterically replaced carbons/carbon substructures in aliphatic structures or real heterocycles [...]

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12

SUZUKI, Toshimitsu, and Yoshihisa WATANABE. "Surface chemistry of carbons. Oxidation reactions of carbon surfaces." Hyomen Kagaku 10, no. 9 (1989): 565–72. http://dx.doi.org/10.1380/jsssj.10.565.

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13

He, Liang-Nian. "Carbon dioxide chemistry: Carbon capture, activation and utilization." Chinese Science Bulletin 66, no. 7 (2021): 713–15. http://dx.doi.org/10.1360/tb-2021-0157.

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14

Bhat, Bilal A., and Bashir A. Shairgojray. "Applications of Micelles in Catalyzing Organic Reactions." Mini-Reviews in Organic Chemistry 17, no. 3 (2020): 289–96. http://dx.doi.org/10.2174/1570193x16666181228112834.

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: Micellar chemistry is gaining considerable interest among organic chemists because these reactions are carried out in environmentally benign solvents like water. Owing to the exhaustive use of toxic solvents in carrying out the different chemical reactions, there is a pressing need for alternative approaches either environmental friendly or having minimum impact on the environment. In this article, we aim to discuss the various aspects of micellar chemistry viz-a-viz its role in guiding the chemical reactions. Micelles help to drive various kinds of organic reactions including oxidations, re

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15

Hazen, R. M., R. T. Downs, A. P. Jones, and L. Kah. "Carbon Mineralogy and Crystal Chemistry." Reviews in Mineralogy and Geochemistry 75, no. 1 (2013): 7–46. http://dx.doi.org/10.2138/rmg.2013.75.2.

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16

YOSHIDA, Yumi. "Carbon Nanomaterials in Analytical Chemistry." Analytical Sciences 34, no. 3 (2018): 257. http://dx.doi.org/10.2116/analsci.34.257.

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17

Boyle, Rebecca. "Carbon rips up chemistry textbooks." New Scientist 233, no. 3108 (2017): 16. http://dx.doi.org/10.1016/s0262-4079(17)30067-2.

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18

Gerin, M., E. Roueff, J. Le Bourlot, et al. "Carbon Chemistry in Photodissociation Regions." Proceedings of the International Astronomical Union 1, S231 (2006): 153. http://dx.doi.org/10.1017/s1743921306007149.

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19

Pelley, Janet. "Better Carbon Capture through Chemistry." ACS Central Science 1, no. 8 (2015): 412–15. http://dx.doi.org/10.1021/acscentsci.5b00352.

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20

Fangmeier, Andreas. "Carbon dioxide chemistry: Environmental issues." Environmental Pollution 91, no. 2 (1996): 267. http://dx.doi.org/10.1016/s0269-7491(96)90045-7.

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21

Harris, Peter. "‘Chemistry and physics of carbon’." Materials Science and Technology 13, no. 12 (1997): 1066. http://dx.doi.org/10.1179/mst.1997.13.12.1066.

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22

DePaolo, Donald, and Ian Bourg. "Chemistry, Geology, and Carbon Mitigation." Accounts of Chemical Research 50, no. 9 (2017): 2055. http://dx.doi.org/10.1021/acs.accounts.7b00349.

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23

NAKASHIMA, Naotoshi. "Chemistry of the Carbon Nanotubes." Kobunshi 54, no. 8 (2005): 572–75. http://dx.doi.org/10.1295/kobunshi.54.572.

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24

SANO, Masahito. "Toward Carbon Nanotube Supramolecular Chemistry." KOBUNSHI RONBUNSHU 59, no. 10 (2002): 565–70. http://dx.doi.org/10.1295/koron.59.565.

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25

Basiuk, Elena V., and Vladimir A. Basiuk. "Green Chemistry of Carbon Nanomaterials." Journal of Nanoscience and Nanotechnology 14, no. 1 (2014): 644–72. http://dx.doi.org/10.1166/jnn.2014.9011.

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26

Lahaye, J. "The chemistry of carbon surfaces." Fuel 77, no. 6 (1998): 543–47. http://dx.doi.org/10.1016/s0016-2361(97)00099-9.

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27

Freund, H. J., and M. W. Roberts. "Surface chemistry of carbon dioxide." Surface Science Reports 25, no. 8 (1996): 225–73. http://dx.doi.org/10.1016/s0167-5729(96)00007-6.

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28

Laskin, Alexander, Julia Laskin, and Sergey A. Nizkorodov. "Chemistry of Atmospheric Brown Carbon." Chemical Reviews 115, no. 10 (2015): 4335–82. http://dx.doi.org/10.1021/cr5006167.

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29

Nienow, Amanda M., and Jeffrey T. Roberts. "HETEROGENEOUS CHEMISTRY OF CARBON AEROSOLS." Annual Review of Physical Chemistry 57, no. 1 (2006): 105–28. http://dx.doi.org/10.1146/annurev.physchem.57.032905.104525.

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30

Rudkevich, Dmitry M., and Heng Xu. "Carbon dioxide and supramolecular chemistry." Chemical Communications, no. 21 (2005): 2651. http://dx.doi.org/10.1039/b500318k.

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31

Baughman, R. H. "CHEMISTRY: Dangerously Seeking Linear Carbon." Science 312, no. 5776 (2006): 1009–110. http://dx.doi.org/10.1126/science.1125999.

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32

TAKEUCHI, Yoshio. "Chemistry of Multifunctional Carbon Compounds." YAKUGAKU ZASSHI 109, no. 11 (1989): 783–801. http://dx.doi.org/10.1248/yakushi1947.109.11_783.

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33

Piantadosi, Claude A. "Biological Chemistry of Carbon Monoxide." Antioxidants & Redox Signaling 4, no. 2 (2002): 259–70. http://dx.doi.org/10.1089/152308602753666316.

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34

Stadlbauer, Wolfgang, and Thomas Kappe. "The Chemistry of Carbon Subsulfide." Sulfur reports 21, no. 4 (1999): 423–45. http://dx.doi.org/10.1080/01961779908047951.

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35

Rance, Graham A., William A. Solomonsz, and Andrei N. Khlobystov. "Click chemistry in carbon nanoreactors." Chemical Communications 49, no. 11 (2013): 1067. http://dx.doi.org/10.1039/c2cc38035h.

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36

Axet, M. R., O. Dechy-Cabaret, J. Durand, M. Gouygou, and P. Serp. "Coordination chemistry on carbon surfaces." Coordination Chemistry Reviews 308 (February 2016): 236–345. http://dx.doi.org/10.1016/j.ccr.2015.06.005.

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37

Somasundaran, P., and L. Xiao. "Chemistry and physics of carbon." Colloids and Surfaces 44 (January 1990): 358. http://dx.doi.org/10.1016/0166-6622(90)80207-k.

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38

Hyatt, I. F. Dempsey, Loma Dave, Navindra David, Kirandeep Kaur, Marly Medard, and Cyrus Mowdawalla. "Hypervalent iodine reactions utilized in carbon–carbon bond formations." Organic & Biomolecular Chemistry 17, no. 34 (2019): 7822–48. http://dx.doi.org/10.1039/c9ob01267b.

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39

Dubinin, M. M., N. S. Polyakov, and G. A. Petukhova. "Porous Structure and Surface Chemistry of Active Carbons." Adsorption Science & Technology 10, no. 1-4 (1993): 17–26. http://dx.doi.org/10.1177/0263617499010001-403.

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The adsorbability on active carbons of substances with different physicochemical properties has been investigated and a comparative analysis of the pore structure parameters of the active carbons as estimated from the sorption of substances with various molecular diameters has been made. The influence of the surface chemistry of carbon sorbents on the adsorption of water vapour has also been studied. The need for a quantitative analysis of the pore structure parameters and the surface chemistry of active carbons as a basis for their universal characterization is discussed.

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40

Kuhlbusch, T. A. J. "OCEAN CHEMISTRY: Enhanced: Black Carbon and the Carbon Cycle." Science 280, no. 5371 (1998): 1903–4. http://dx.doi.org/10.1126/science.280.5371.1903.

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41

Teyssier, D., D. Fossé, M. Gerin, J. Pety, A. Abergel, and E. Roueff. "Carbon budget and carbon chemistry in Photon Dominated Regions." Astronomy & Astrophysics 417, no. 1 (2004): 135–49. http://dx.doi.org/10.1051/0004-6361:20034534.

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42

Mondal, Animesh, and Chhanda Mukhopadhyay. "Construction of Carbon-Carbon and Carbon-Heteroatom Bonds: Enabled by Visible Light." Current Organic Chemistry 24, no. 1 (2020): 44–73. http://dx.doi.org/10.2174/1385272824666200211115154.

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The present review provides an overview of visible light-mediated environment- friendly approaches over the past decade for the formation of carbon-carbon and carbon-heteroatom framework. This area has recently emerged as a versatile, environmentally benign and green platform for the development of a highly sustainable synthetic methodology. According to the recent advancements, visible light has come to the forefront in synthetic organic chemistry as a powerful green strategy for the activation of small molecules.

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43

Salzer, A. "Nomenclature of Organometallic Compounds of the Transition Elements (IUPAC Recommendations 1999)." Pure and Applied Chemistry 71, no. 8 (1999): 1557–85. http://dx.doi.org/10.1351/pac199971081557.

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Organometallic compounds are defined as containing at least one metal-carbon bond between an organic molecule, ion, or radical and a metal. Organometallic nomenclature therefore usually combines the nomenclature of organic chemisty and that of coordination chemistry. Provisional rules outlining nomenclature for such compounds are found both in Nomenclature of Organic Chemistry, 1979 and in Nomenclature of Inorganic Chemistry, 1990This document describes the nomenclature for organometallic compounds of the transition elements, that is compounds with metal-carbon single bonds, metal-carbon multi

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44

Sugimoto, Hiroshi, and Shohei Inoue. "Recent progress in the synthesis of polymers based on carbon dioxide." Pure and Applied Chemistry 78, no. 10 (2006): 1823–34. http://dx.doi.org/10.1351/pac200678101823.

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The alternating copolymerization of carbon dioxide and epoxide to give polycarbonate has attracted the attention of many chemists, because it is one of the most promising methodologies for the utilization of carbon dioxide as a safe, clean, and abundant raw material in the synthetic chemistry. Recent developments of the catalysts for the alternating copolymerization are based on the rational design of metal complexes, especially complexes of transition metal with well-defined structures.

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45

Sheka, Elena F. "sp2 Carbon Stable Radicals." C 7, no. 2 (2021): 31. http://dx.doi.org/10.3390/c7020031.

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sp2 Nanocarbons such as fullerenes, carbon nanotubes, and graphene molecules are not only open-shell species, but spatially extended, due to which their chemistry is quite specific. Cogently revealed dependence of the final products composition on size and shape of the carbons in use as well as on the chemical prehistory is accumulated in a particular property—the stabilization of the species’ radical efficiency, thus providing the matter of stable radicals. If the feature is highly restricted and rarely available in ordinary chemistry, in the case of sp2 nanocarbons it is just an ordinary eve

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46

Kerru, Nagaraju, Suresh Maddila, and Sreekantha B. Jonnalagadda. "Design of Carbon-carbon and Carbon-heteroatom Bond Formation Reactions under Green Conditions." Current Organic Chemistry 23, no. 28 (2020): 3154–90. http://dx.doi.org/10.2174/1385272823666191202105820.

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: The development of C-C and C-heteroatom (C-N, C-O and C-P) bond reactions is a field of significant interest and has received momentous attention in modern organic chemistry. These reactions have been exploited in the synthesis of pharmaceuticals, agrochemicals and molecules of interest in materials science. With the increasing awareness of global warming and the use of renewable energies, it is of paramount importance to reduce the usage of hazardous chemicals in both industrial and academic research and to achieve a healthier environment through green practices. Green chemistry is a rapidl

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47

Honek, John F. "Biological chemistry of the carbon–sulfur bond." Canadian Journal of Chemistry 93, no. 10 (2015): 1051–60. http://dx.doi.org/10.1139/cjc-2015-0270.

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Carbon–sulfur biological chemistry encompasses a fascinating area of biochemistry and medicinal chemistry and includes the roles that methionine and S-adenosyl-l-methionine play in cells as well as the chemistry of intracellular thiols such as glutathione. This article, based on the 2014 Bernard Belleau Award lecture, provides an overview of some of the key investigations that were undertaken in this area from a bioorganic perspective. The research has ameliorated our fundamental knowledge of several of the enzymes utilizing these sulfur-containing molecules, has led to the development of seve

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48

Liu, Qinghe, Chuanfa Ni, and Jinbo Hu. "China's flourishing synthetic organofluorine chemistry: innovations in the new millennium." National Science Review 4, no. 3 (2017): 303–25. http://dx.doi.org/10.1093/nsr/nwx058.

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Abstract The new millennium has witnessed the rapid development of synthetic organofluorine chemistry all over the world, and chemists in China have made significant contributions in this field. This review aims to provide a brief introduction to China's primary innovations from 2000 to early 2017, covering fluorination, fluoroalkylation, fluoromethylthiolation, fluoroolefination and polyfluoroarylation, as well as synthesis with fluorinated building blocks. Recent advances in the chemistry of difluorocarbene and the chemistry of carbon–fluorine bond activation are also discussed. As a conclus

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49

Uchiyama, Shunichi. "Innovation of Coulometric Analysis, Based on Carbon Felt Electrodes and its Application to Bioelectroanalytical Chemistry." Review of Polarography 58, no. 2 (2012): 67–73. http://dx.doi.org/10.5189/revpolarography.58.67.

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50

Vytřas, Karel, Ivan Svancara, and Radovan Metelka. "Carbon paste electrodes in electroanalytical chemistry." Journal of the Serbian Chemical Society 74, no. 10 (2009): 1021–33. http://dx.doi.org/10.2298/jsc0910021v.

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An overview is given dealing with the applications of carbon paste electrodes in equilibrium potentiometry as well as in electrochemical stripping analysis using both voltammetric and potentiometric modes. Various modifications of carbon pastes and carbon paste-based biosensors are also mentioned. The main emphasis in this article is directed at summarizing recent results of the authors' research group during the past few years.

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