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Journal articles on the topic 'Chemistry, nomenclature'

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Published: 4 June 2021

Last updated: 4 March 2023

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1

Novák, Miroslav. "Brief Outline of the History of Chemical Nomenclature." Chemické listy 116, no. 10 (October 15, 2022): 617–25. http://dx.doi.org/10.54779/chl20220617.

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Chemical terminology and nomenclature form an important part of chemistry. Apart from verbal terms, the important and inseparable part of nomenclature consists of symbols – logograms. They substitute names of elements and compounds and in modern nomenclatures represent their atomic or molecular weights. Old nomenclatures, first of all the alchemic one, were greatly redundant and unsystematic and used many non-compatible logograms. The first systematic nomenclature, completed by the logogram system, was created by de Morveau, Lavoisier, Berthollet, and Fourcroy (1787). The system of plausible alphabetic logograms was introduced by Berzelius (1812). The first Czech systemic nomenclature was created by Presl (1828) using only five valency suffixes; the improved nomenclature by Šafařík (1860) expressed all oxidation numbers by the word suffixes. The modern Czech chemical nomenclature tends to accept most IUPAC recommendations.

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2

Salzer, A. "Nomenclature of Organometallic Compounds of the Transition Elements (IUPAC Recommendations 1999)." Pure and Applied Chemistry 71, no. 8 (August 30, 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 multiple bonds as well as complexes with unsaturated molecules (metal-p-complexes).Organometallic compounds are considered to be produced by addition reactions and so they are named on an addition principle. The name therefore is built around the central metal atom name. Organic ligand names are derived according to the rules of organic chemistry with appropriate endings to indicate the different bonding modes. To designate the points of attachment of ligands in more complicated structures, the h, k, and m-notations are used. The final section deals with the abbreviated nomenclature for metallocenes and their derivatives.ContentsIntroduction Systems of Nomenclature2.1 Binary type nomenclature 2.2 Substitutive nomenlcature 2.3 Coordination nomenclature Coordination Nomenclature3.1 General definitions of coordination chemistry 3.2 Oxidation numbers and net charges 3.3 Formulae and names for coordination compounds Nomenclature for Organometallic Compounds of Transition Metals 4.1 Valence-electron-numbers and the 18-valence-electron-rule 4.2 Ligand names 4.2.1 Ligands coordinating by one metal-carbon single bond 4.2.2 Ligands coordinating by several metal-carbon single bonds 4.2.3 Ligands coordinating by metal-carbon multiple bonds 4.2.4 Complexes with unsaturated molecules or groups 4.3 Metallocene nomenclature

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3

Pekov, Igor V., Sergey V. Krivovichev, Andrey A. Zolotarev, Viktor N. Yakovenchuk, Thomas Armbruster, and Yakov A. Pakhomovsky. "Crystal chemistry and nomenclature of the lovozerite group." European Journal of Mineralogy 21, no. 5 (October 30, 2009): 1061–71. http://dx.doi.org/10.1127/0935-1221/2009/0021-1957.

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4

Giles, P. M. "Revised Section F: Natural products and related compounds." Pure and Applied Chemistry 71, no. 4 (January 1, 1999): 587–643. http://dx.doi.org/10.1351/pac199971040587.

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The nomenclature of natural products has suffered from much confusion, mostly for historical reasons. The isolation of a new substance, in the early days of the science, generally preceded its characterization by a lengthy period. Thus, these compounds were often assigned trivial names that gave no indication of the structure of the molecule and were often found afterwards to be misleading. Even when the original names were later revised (for example: glycerin to glycerol) the new names often expressed the structure imperfectly and were thus unsuitable for the nomenclatural manipulation that is required to name derivatives or stereoisomers. The result was a proliferation of trivial names that taxed the memory of chemists and obscured important structural relationships.The resultant disorder in the literature led to the creation of committees of specialists with the task of codifying the naming of compounds in various connected areas of natural-product chemistry, such as steroids, lipids, and carbohydrates. As far as their recommendations have been followed, their efforts have been successful in eliminating confusing or duplicate nomenclature.It is the aim of the lUPAC Commission on Nomenclature of Organic Chemistry to unite as far as possible all the specialist reports into a single set of recommendations that can be applied in most areas of natural-product chemistry. Accordingly, provisional recommendations were prepared and published as Section F of the lUPAC Organic Nomenclature Rules, first in 1976, and then in the 1979 edition of the Rules.

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5

Golub, A. "CHEMICAL TERMINOLOGY AND NOMENCLATURE OF COORDINATION CHEMISTRY." Bulletin of Taras Shevchenko National University of Kyiv. Chemistry, no. 1(55) (2018): 6–8. http://dx.doi.org/10.17721/1728-2209.2018.1(55).1.

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Ukrainian chemical terminology is one of the most advanced in the world, due to the rapid development after the rise of independence and it basing on the latest developments of IUPAC terminology and nomenclature. First of all, it is owed to the fundamental principles developed by our predecessors, who, in the difficult times of Soviet power, overcoming the impenetrable walls of imperial resistance, nevertheless tried to promote the development of chemical terminology in the course of time, and sometimes ahead of the advanced international and national terminology of others, even free countries. The orientation on the international terminology standards was chosen to build a new Ukrainian terminology and nomenclature at the Department of Inorganic Chemistry of Shevchenko University of Kyiv in the 50's – 70's of the 20th century The basic requirements for the terminology and nomenclature of inorganic chemistry were formulated, which can be used as a guide for the development of Ukrainian chemical terminology and nomenclature nowadays: 1.Chemical terms should correspond to the modern meaning. 2. The nomenclature of inorganic compounds and elements should be consistent with the foundations of inorganic chemistry. 3. The nomenclature should be developed in close connection with the systematics of chemical elements and compounds. 4. The new Ukrainian nomenclature in inorganic chemistry should be based on the international nomenclature. 5. When creating a new nomenclature it is necessary to take into account the specifics of the Ukrainian language. 6. The nomenclature should be rational and give unambiguous names of chemical compounds. 7. The transfer of terms and names from other languages should be created according to the phonetic principle and transcribed from the original language. The most important principles of Ukrainian chemical terminology and nomenclature of coordination chemistry have been discussed, examples of the possibilities of adaptation of the IUPAC nomenclature rules on the basis of the Ukrainian language have been demonstrated.

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6

FUENTES-ARDERIU, JAVIER. "International Nomenclature in Clinical Chemistry." Annals of Internal Medicine 106, no. 6 (June 1, 1987): 915. http://dx.doi.org/10.7326/0003-4819-106-6-915_2.

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7

Wilson, M. A. "Systematic Nomenclature of Organic Chemistry." Organic Geochemistry 32, no. 9 (September 2001): 1175. http://dx.doi.org/10.1016/s0146-6380(01)00078-x.

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8

Fox, Robert B. "Nomenclature of Polymeric Materials." Rubber Chemistry and Technology 68, no. 3 (July 1, 1995): 547–50. http://dx.doi.org/10.5254/1.3538755.

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Abstract The purpose of this brief review is to aquaint the authors and readers of Rubber Chemistry and Technology with the essentials of polymer nomenclature. To ensure quality communication, it is important that a common language be utilized that is understood, not only by those in the rubber and elastomers field, but by anyone in related areas of polymer science and technology as well. Traditional and trade names of polymeric materials often have time-honored meanings but are obscure or incomplete and frequently fail to convey reasonably accurate information. Many polymer and chemical names are at best ambiguous, but are easily correctable. The methods outlined here have been adopted by the Commission on Macromolecular Nomenclature of the International Union of Pure and Applied Chemistry (IUPAC); their use in Rubber Chemistry and Technology is strongly recommended. Additional details will be found in the appropriate IUPAC publications. Note that for the purposes of this paper italics are generally used to set-off “names” for emphasis. However, when naming polymers for RC&T, Roman characters should generally be used with only the ‘connectives’ or ‘prefixes’ appearing in italics (see Table I). By convention, in manuscripts text that is to be printed in italics should be underlined.

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9

Fuentes-Arderiu, X. "Standardization of nomenclature in clinical chemistry." Clinical Chemistry 35, no. 7 (July 1, 1989): 1552. http://dx.doi.org/10.1093/clinchem/35.7.1552a.

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10

Palacios, Joaquin. "Octachem Model: Organic Chemistry Nomenclature Companion." Journal of Chemical Education 83, no. 6 (June 2006): 890. http://dx.doi.org/10.1021/ed083p890.

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11

Kauffman, George B. "Nomenclature of inorganic chemistry : Recommendations 1990." Polyhedron 10, no. 15 (January 1991): 1843–44. http://dx.doi.org/10.1016/s0277-5387(00)83810-3.

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12

Eaborn, Colin. "Nomenclature of Inorganic Chemistry: Recommendations 1990." Journal of Organometallic Chemistry 405, no. 3 (March 1991): C48. http://dx.doi.org/10.1016/0022-328x(91)86303-8.

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13

Fresenius, Philipp, and Klaus Goerlitzer. "ChemInform Abstract: Nomenclature in Organic Chemistry." ChemInform 30, no. 9 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199909025.

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14

Leigh, G. Jeffery. "A History of CNIC." Chemistry International 41, no. 3 (July 1, 2019): 39–43. http://dx.doi.org/10.1515/ci-2019-0313.

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Abstract The systematic nomenclature of inorganic chemistry is much older than IUPAC itself, and so is the history of the Commission for the Nomenclature of Inorganic Chemistry (CNIC). The nomenclature developed as new chemistry originated and grew at the beginning of the 19th century, when the chemical community came to recognise the need for international agreement on the formalisms to be used, to enable practitioners from different countries to understand communications between them. In that period such communications were only written or printed. Since CNIC produced the first of its IUPAC Red Books on the nomenclature of inorganic chemistry in 1957, the Red Books themselves have been continuously rewritten and expanded as the science of chemistry has grown, and they represent a collaborative production, both in the number of people involved and the time-frame they occupy, which is possibly unique in modern science.

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15

曹, 忠民. "Studies on the International Nomenclature of Organic Chemistry: (II) Modern Substitutive Nomenclature." Journal of Organic Chemistry Research 05, no. 03 (2017): 142–52. http://dx.doi.org/10.12677/jocr.2017.53019.

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16

Reinhardt, Carsten. "IUPAC Engagement in the Instrumental Revolution." Chemistry International 41, no. 3 (July 1, 2019): 35–38. http://dx.doi.org/10.1515/ci-2019-0312.

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Abstract In the second half of the Twentieth Century, the chemical and molecular sciences experienced a deep transformation with regard to the types of research instruments used, and the associated methods involved. Historians have coined this development the Instrumental Revolution, and even described it as the Second Chemical Revolution [1]. With the latter notion, they referred to the First Chemical Revolution of the late eighteenth century, when Antoine Laurent Lavoisier and his allies transformed chemistry’s theoretical framework along with its nomenclature, creating modern chemistry. The “second” chemical revolution of the twentieth century had an equally deep impact on chemistry’s theoretical base, linking chemistry to quantum physics, and expanding its range into the life sciences and technologies, the material sciences, and engineering. However, the related changes in terminology and nomenclature have largely escaped the historian’s attention, and this might explain why IUPAC’s role in the Instrumental Revolution has not been investigated in any detail. In the following, I will first briefly describe the Instrumental Revolution, and its main impact on chemistry and related fields, before sketching IUPAC’s role in facilitating and enhancing it [2].

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17

Gluschenko, Viktor. "Terminology and nomenclature in oil-field chemistry." Вестник Пермского национального исследовательского политехнического университета. Геология. Нефтегазовое и горное дело 12 (2014): 93–97. http://dx.doi.org/10.15593/2224-9923/2014.12.11.

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18

van Grieken, R., and M. de Bruin. "Nomenclature for radioanalytical chemistry (IUPAC Recommendations 1994)." Pure and Applied Chemistry 66, no. 12 (January 1, 1994): 2513–26. http://dx.doi.org/10.1351/pac199466122513.

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19

DERMER, O. C. "Lighthearted Nomenclature: Organic Chemistry: The Name Game." Science 239, no. 4844 (March 4, 1988): 1184–85. http://dx.doi.org/10.1126/science.239.4844.1184.

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20

Hartshorn, Richard M., Karl-Heinz Hellwich, Andrey Yerin, Ture Damhus, and Alan T. Hutton. "Brief guide to the nomenclature of inorganic chemistry." Pure and Applied Chemistry 87, no. 9-10 (October 1, 2015): 1039–49. http://dx.doi.org/10.1515/pac-2014-0718.

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AbstractThis IUPAC Technical Report (PAC-REP-14-07-18) is one of a series that seeks to distil the essentials of IUPAC nomenclature recommendations. The present report provides a succinct summary of material presented in the publication Nomenclature of Inorganic Chemistry – IUPAC Recommendations 2005. The content of this report will be republished and disseminated as a four-sided lift-out document (see supplementary information) which will be available for inclusion in textbooks and similar publications.

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21

Shchipalkina, Nadezhda V., Igor V. Pekov, Nikita V. Chukanov, Cristian Biagioni, and Marco Pasero. "Crystal chemistry and nomenclature of rhodonite-group minerals." Mineralogical Magazine 83, no. 6 (October 9, 2019): 829–35. http://dx.doi.org/10.1180/mgm.2019.65.

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AbstractThis paper presents the nomenclature of the rhodonite group accepted by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA). An overview of the previous studies of triclinic (space group P$\bar{1}$) pyroxenoids belonging to the rhodonite structure type, with a focus on their crystal chemistry, is given. These minerals have the general structural formula VIIM(5)VIM(1)VIM(2)VIM(3)VIM(4)[Si5O15]. The following dominant cations at the M sites are known at present: M(5) = Ca or Mn2+, M(1–3) = Mn2+; and M(4) = Mn2+ or Fe2+. In accordance with the nomenclature, the rhodonite group consists of three IMA-approved mineral species having the following the general chemical formulae: M(5)AM(1–3)B3M(4)C[Si5O15], where A = Ca or Mn2+; B = Mn2+; and C = Mn2+ or Fe2+. The end-member formulae of approved rhodonite-group minerals are as follows: rhodonite CaMn3Mn[Si5O15]; ferrorhodonite CaMn3Fe[Si5O15]; and vittinkiite MnMn3Mn[Si5O15].

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22

Shaw, David B., and Laura R. Yindra. "Organic Nomenclature." Journal of Chemical Education 80, no. 10 (October 2003): 1223. http://dx.doi.org/10.1021/ed080p1223.

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23

Shaw, David. "Inorganic Nomenclature." Journal of Chemical Education 80, no. 6 (June 2003): 711. http://dx.doi.org/10.1021/ed080p711.1.

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24

Shaw, David B. "Organic Nomenclature." Journal of Chemical Education 71, no. 5 (May 1994): 421. http://dx.doi.org/10.1021/ed071p421.2.

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25

ten Hoor, Marten J. "Inorganic Nomenclature." Journal of Chemical Education 73, no. 8 (August 1996): 825. http://dx.doi.org/10.1021/ed073p825.

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26

Shaw, David B. "Inorganic Nomenclature." Journal of Chemical Education 70, no. 12 (December 1993): 978. http://dx.doi.org/10.1021/ed070p978.2.

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27

Contreras-García, J., F. Izquierdo-Ruiz, M. Marqués, and F. J. Manjón. "Borates or phosphates? That is the question." Acta Crystallographica Section A Foundations and Advances 76, no. 2 (February 25, 2020): 197–205. http://dx.doi.org/10.1107/s2053273319016826.

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Chemical nomenclature is perceived to be a closed topic. However, this work shows that the identification of polyanionic groups is still ambiguous and so is the nomenclature for some ternary compounds. Two examples, boron phosphate (BPO4) and boron arsenate (BAsO4), which were assigned to the large phosphate and arsenate families, respectively, nearly a century ago, are explored. The analyses show that these two compounds should be renamed phosphorus borate (PBO4) and arsenic borate (AsBO4). Beyond epistemology, this has pleasing consequences at several levels for the predictive character of chemistry. It paves the way for future work on the possible syntheses of SbBO4 and BiBO4, and it also renders previous structure field maps completely predictive, allowing us to foresee the structure and phase transitions of NbBO4 and TaBO4. Overall, this work demonstrates that quantum mechanics calculations can contribute to the improvement of current chemical nomenclature. Such revisitation is necessary to classify compounds and understand their properties, leading to the main final aim of a chemist: predicting new compounds, their structures and their transformations.

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28

DR ARIJIT DAS, DR ARIJIT DAS. "New Innovative Methods for IUPAC Nomenclature of Bicyclo and Spiro Compounds in Organic Chemistry." Indian Journal of Applied Research 3, no. 7 (October 1, 2011): 596–97. http://dx.doi.org/10.15373/2249555x/july2013/189.

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29

Kay, Colin D., Michael N. Clifford, Pedro Mena, Gordon J. McDougall, Cristina Andres-Lacueva, Aedin Cassidy, Daniele Del Rio, et al. "Recommendations for standardizing nomenclature for dietary (poly)phenol catabolites." American Journal of Clinical Nutrition 112, no. 4 (September 16, 2020): 1051–68. http://dx.doi.org/10.1093/ajcn/nqaa204.

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ABSTRACT There is a lack of focus on the protective health effects of phytochemicals in dietary guidelines. Although a number of chemical libraries and databases contain dietary phytochemicals belonging to the plant metabolome, they are not entirely relevant to human health because many constituents are extensively metabolized within the body following ingestion. This is especially apparent for the highly abundant dietary (poly)phenols, for which the situation is compounded by confusion regarding their bioavailability and metabolism, partially because of the variety of nomenclatures and trivial names used to describe compounds arising from microbial catabolism in the gastrointestinal tract. This confusion, which is perpetuated in online chemical/metabolite databases, will hinder future discovery of bioactivities and affect the establishment of future dietary guidelines if steps are not taken to overcome these issues. In order to resolve this situation, a nomenclature system for phenolic catabolites and their human phase II metabolites is proposed in this article and the basis of its format outlined. Previous names used in the literature are cited along with the recommended nomenclature, International Union of Pure and Applied Chemistry terminology, and, where appropriate, Chemical Abstracts Service numbers, InChIKey, and accurate mass.

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30

Hellwich, Karl-Heinz, Richard M. Hartshorn, Andrey Yerin, Ture Damhus, and Alan T. Hutton. "Brief guide to the nomenclature of organic chemistry (IUPAC Technical Report)." Pure and Applied Chemistry 92, no. 3 (March 26, 2020): 527–39. http://dx.doi.org/10.1515/pac-2019-0104.

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AbstractThis IUPAC Technical Report is one of a series that seeks to distil the essentials of IUPAC nomenclature recommendations. The present report provides a succinct summary of material presented in the publication Nomenclature of Organic Chemistry – IUPAC Recommendations and Preferred Names 2013. The content of this report will be republished and disseminated as a four-sided lift-out document (see supplementary information) which will be available for inclusion in textbooks and similar publications.

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31

Heping, Sun, and Wu Yulin. "Chinese Nomenclature of Substituent Groups in Organic Chemistry." University Chemistry 30, no. 2 (2015): 61–63. http://dx.doi.org/10.3866/pku.dxhx20150261.

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32

Hatert, Frédéric, Edward S. Grew, Pietro Vignola, Nicola Rotiroti, Fabrizio Nestola, Paul Keller, Maxime Baijot, et al. "Crystal chemistry and nomenclature of fillowite-type phosphates." Canadian Mineralogist 59, no. 4 (July 1, 2021): 781–96. http://dx.doi.org/10.3749/canmin.2000043.

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ABSTRACT The crystal chemistries of five samples of minerals belonging to the fillowite group were structurally investigated: (A) fillowite from the Buranga pegmatite, Rwanda; (B) fillowite from the Kabira pegmatite, Uganda; (C) johnsomervilleite from Loch Quoich, Scotland; (D) johnsomervilleite from the Malpensata pegmatite, Italy; and (E) chladniite from the Sapucaia pegmatite, Minas Gerais, Brazil. Their crystal structures were refined in space group R (No. 148), using single-crystal X-ray diffraction data, to R1 values of (A) 3.79%, (B) 3.52%, (C) 4.14%, (D) 4.04%, and (E) 5.59%. Unit-cell parameters are: (A) a = 15.122(1), c = 43.258(4) Å; (B) a = 15.125(1), c = 43.198(3) Å; (C) a = 15.036(2), c = 42.972(9) Å; (D) a = 15.090(2), c = 43.050(9) Å; and (E) a = 15.1416(6), c = 43.123(2) Å. The asymmetric unit contains 15 cation sites with coordinations ranging from V to IX, as well as six P sites. The complex structure can be split into three types of chains running parallel to the c axis. These chains are composed of edge- and face-sharing polyhedra. Detailed cation distributions were determined for all five samples, and their comparison allowed us to establish the general formula A3BC11(PO4)9 for fillowite-type phosphates, where A represents the group of sites mainly occupied by Na, B the Ca sites, and C the sites containing the divalent cations Fe2+, Mn, and Mg. This formula was accepted by the CNMNC, and the four valid mineral species occurring in the fillowite group are fillowite (C = Mn), johnsomervilleite (C = Fe2+), chladniite (C = Mg), and galileiite (B and C = Fe2+). Stornesite-(Y) is discredited, since this mineral corresponds to Y-bearing chladniite.

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33

Mikhailov, O. V. "Nomenclature and Terminology Problems of Modern Coordination Chemistry." Russian Journal of General Chemistry 88, no. 6 (June 2018): 1337–48. http://dx.doi.org/10.1134/s1070363218060452.

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34

Moss, G. P. "A history of the nomenclature of organic chemistry." Endeavour 10, no. 1 (January 1986): 56. http://dx.doi.org/10.1016/0160-9327(86)90086-4.

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35

Horwitz, W. "Nomenclature for sampling in analytical chemistry (Recommendations 1990)." Pure and Applied Chemistry 62, no. 6 (January 1, 1990): 1193–208. http://dx.doi.org/10.1351/pac199062061193.

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36

BANKS, R. E., and J. C. TATLOW. "ChemInform Abstract: Organofluorine Chemistry: Nomenclature and Historical Landmarks." ChemInform 26, no. 31 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199531295.

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37

Ericsson, Inger, and RobertP Lattimer. "Pyrolysis nomenclature." Journal of Analytical and Applied Pyrolysis 14, no. 4 (February 1989): 219–21. http://dx.doi.org/10.1016/0165-2370(89)80001-4.

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38

Wirtz, Michael C., Joan Kaufmann, and Gary Hawley. "Nomenclature Made Practical: Student Discovery of the Nomenclature Rules." Journal of Chemical Education 83, no. 4 (April 2006): 595. http://dx.doi.org/10.1021/ed083p595.

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39

McNaught, Alan D. "Nomenclature of carbohydrates." Carbohydrate Research 297, no. 1 (January 1997): 1–92. http://dx.doi.org/10.1016/s0008-6215(97)83449-0.

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40

JCBN. "Nomenclature of glycolipids." Carbohydrate Research 312, no. 4 (November 1998): 167–75. http://dx.doi.org/10.1016/s0008-6215(98)00231-6.

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41

Eliel, Ernest L. "Infelicitous stereochemical nomenclature." Chirality 9, no. 5-6 (1997): 428–30. http://dx.doi.org/10.1002/(sici)1520-636x(1997)9:5/6<428::aid-chir5>3.0.co;2-1.

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42

Bayliss, P. "Cesium kupletskite renamed kupletskite-(Cs)." Mineralogical Magazine 71, no. 3 (June 2007): 365–67. http://dx.doi.org/10.1180/minmag.2007.071.3.365.

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AbstractCesium kupletskite has been renamed kupletskite-(Cs) with the approval of the IMA Commission on New Minerals, Nomenclature and Classification, because the name of a mineral species should be a single word and the International Union of Pure and Applied Chemistry spelling is caesium. The presence or absence of parentheses around the suffix chemical-element is discussed. The advantages of the chemical-element suffix nomenclature are stated.

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43

LIN, Qi, Li-Yun YAO, and Ruo-Lin YANG. "Some Nomenclature Problems in Teaching of Medicinal Organic Chemistry." University Chemistry 32, no. 3 (2017): 55–59. http://dx.doi.org/10.3866/pku.dxhx201608025.

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44

Marconi, Andrea M., Noemi Proietti, and Errico Zeuli. "Computer aided nomenclature: The MARK algorithm for organic chemistry." Tetrahedron Computer Methodology 3, no. 5 (1990): 297–303. http://dx.doi.org/10.1016/0898-5529(90)90106-i.

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45

Buenzli-Trepp, Ursula. "ChemInform Abstract: Nomenclature in Organic, Organometal and Coordination Chemistry." ChemInform 32, no. 50 (May 23, 2010): no. http://dx.doi.org/10.1002/chin.200150223.

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46

Kurniawan, C., M. Dhiyaulkhaq, N. Wijayati, K. Kasmui, D. Nasekhah, and M. H. Ismail. "Android-Based Mobile Learning Application Design: Its Implementation and Evaluation for Aiding Secondary School Students' to Study Inorganic Compound Nomenclature." Jurnal Pendidikan IPA Indonesia 11, no. 3 (September 30, 2022): 469–76. http://dx.doi.org/10.15294/jpii.v11i3.38243.

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Inorganic compound nomenclature is one of the most basic concepts in chemistry. Therefore, for students, correct naming of the chemicals is essential before learning advanced chemistry. However, nomenclature as a learning topic consists of rules and thus requires frequent practice. Tenth graders will face difficulties if they have remember thousands of the chemicals' names. The objective of this research is to develop and validate the effectiveness of android-based learning media to help students in learning chemical compound nomenclature. In order to meet the goal, this study was conducted in stages; they are (1) information collection, (2) planning, (3) product draft development, (4) small-scale trials, (5) product revisions, and (6) large-scale trials. The effectiveness of the examined mobile-app was measured using post-test questions, resulting in 87.88% student completion. Furthermore, since experts have been in agreement concerning the validity of the examined mobile app – both the content and the media, the app can be used for learning process.

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Constable. "What's in a Name?—A Short History of Coordination Chemistry from Then to Now." Chemistry 1, no. 1 (August 22, 2019): 126–63. http://dx.doi.org/10.3390/chemistry1010010.

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This article traces the development of coordination chemistry and shows how progress in the science has been paralleled by the development of a vocabulary and nomenclature to describe new concepts, structural features and compound types.

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48

Fogg, Arnold G. "Nomenclature of stripping voltammetry." Analytical Proceedings including Analytical Communications 32, no. 10 (1995): 433. http://dx.doi.org/10.1039/ai9953200433.

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Heusler, K. E., D. Landolt, and S. Trasatti. "Electrochemical corrosion nomenclature." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 274, no. 1-2 (December 1989): 345–48. http://dx.doi.org/10.1016/0022-0728(89)87063-9.

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Ehrenhauser, Franz S. "PAH and IUPAC Nomenclature." Polycyclic Aromatic Compounds 35, no. 2-4 (January 26, 2015): 161–76. http://dx.doi.org/10.1080/10406638.2014.918551.

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