Г. А. Альпер

419 total citations
40 papers, 350 citations indexed

About

Г. А. Альпер is a scholar working on Spectroscopy, Fluid Flow and Transfer Processes and Biomedical Engineering. According to data from OpenAlex, Г. А. Альпер has authored 40 papers receiving a total of 350 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Spectroscopy, 17 papers in Fluid Flow and Transfer Processes and 16 papers in Biomedical Engineering. Recurrent topics in Г. А. Альпер's work include Thermodynamic properties of mixtures (17 papers), Analytical Chemistry and Chromatography (15 papers) and Phase Equilibria and Thermodynamics (13 papers). Г. А. Альпер is often cited by papers focused on Thermodynamic properties of mixtures (17 papers), Analytical Chemistry and Chromatography (15 papers) and Phase Equilibria and Thermodynamics (13 papers). Г. А. Альпер collaborates with scholars based in Russia, India and Spain. Г. А. Альпер's co-authors include R. S. Kumeev, I. V. Terekhova, Ilya A. Khodov, G. M. Mamardashvili, Sergey V. Efimov, Vladimir V. Klochkov, Н. Ж. Мамардашвили, Luís A. E. Batista de Carvalho, N. Georgi and М. Г. Киселев and has published in prestigious journals such as Chemical Physics Letters, Carbohydrate Polymers and RSC Advances.

In The Last Decade

Г. А. Альпер

39 papers receiving 346 citations

Peers

Г. А. Альпер

SPECT

Xiaomei Qiu China

Jonathan J. Booth United Kingdom

М. А. Krest’yaninov Russia

Fernando Pulidori Italy

Vladimir P. Kazachenko Russia

Maryvonne Luçon France

N. G. Manin Russia

Ramamurthy Palepu Canada

Epaminondas B. Leodidis United States

Takuji Sugimoto Japan

Xiaomei Qiu China

Г. А. Альпер

185 ×1.2

SPECT

144 ×1.1

71 ×0.8

37 ×0.5

44 ×0.8

Citations per year, relative to Г. А. Альпер Г. А. Альпер (= 1×) peers Xiaomei Qiu

Countries citing papers authored by Г. А. Альпер

Since Specialization

Citations

This map shows the geographic impact of Г. А. Альпер's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Г. А. Альпер with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Г. А. Альпер more than expected).

Fields of papers citing papers by Г. А. Альпер

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Г. А. Альпер. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Г. А. Альпер. The network helps show where Г. А. Альпер may publish in the future.

Co-authorship network of co-authors of Г. А. Альпер

This figure shows the co-authorship network connecting the top 25 collaborators of Г. А. Альпер. A scholar is included among the top collaborators of Г. А. Альпер based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Г. А. Альпер. Г. А. Альпер is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Альпер, Г. А., et al.. (2016). Influence of molecular association on the solubility of methylxanthines in supercritical solvent CO2–methanol. Russian Journal of Physical Chemistry B. 10(7). 1166–1170. 5 indexed citations

Terekhova, I. V., R. S. Kumeev, Г. А. Альпер, et al.. (2016). Molecular recognition of aromatic carboxylic acids by hydroxypropyl-γ-cyclodextrin: experimental and theoretical evidence. RSC Advances. 6(55). 49567–49577. 14 indexed citations

Khodov, Ilya A., Г. А. Альпер, G. M. Mamardashvili, & Н. Ж. Мамардашвили. (2015). Hybrid multi-porphyrin supramolecular assemblies: Synthesis and structure elucidation by 2D DOSY NMR studies. Journal of Molecular Structure. 1099. 174–180. 33 indexed citations

Khodov, Ilya A., Sergey V. Efimov, Vladimir V. Klochkov, Г. А. Альпер, & Luís A. E. Batista de Carvalho. (2014). Determination of preferred conformations of ibuprofen in chloroform by 2D NOE spectroscopy. European Journal of Pharmaceutical Sciences. 65. 65–73. 38 indexed citations

Khodov, Ilya A., et al.. (2014). Synthesis and spectroscopic characterization of Ru(II) and Sn(IV)-porphyrins supramolecular complexes. Journal of Molecular Structure. 1081. 426–430. 19 indexed citations

Terekhova, I. V., et al.. (2014). Cyclodextrin–benzoic acid binding in salt solutions: Effects of biologically relevant anions. Carbohydrate Polymers. 110. 472–479. 7 indexed citations

Terekhova, I. V., et al.. (2012). Role of biologically active inorganic anions Cl− and Br− in inclusion complex formation of α-cyclodextrin with some aromatic carboxylic acids. Chemical Physics Letters. 557. 134–139. 8 indexed citations

Terekhova, I. V., Małgorzata Koźbiał, R. S. Kumeev, & Г. А. Альпер. (2011). Inclusion Complex Formation Between Modified Cyclodextrins and Riboflvin and Alloxazine in Aqueous Solution. Journal of Solution Chemistry. 40(8). 1435–1446. 13 indexed citations

Mamardashvili, G. M., et al.. (2011). Solubility of porphyrin macrocycles in mixed solvents. Journal of Structural Chemistry. 52(2). 304–309. 8 indexed citations

10.

Альпер, Г. А., et al.. (2010). The viscosity of the methanol-n-decane system in the region of low n-decane concentrations. Russian Journal of Physical Chemistry A. 84(6). 950–953. 2 indexed citations

11.

Lebedevа, N. Sh., et al.. (2009). Photoinduced isomerization of 4-(4′-dimethylaminostyryl) pyridine N-oxide. Journal of Structural Chemistry. 50(4). 722–726.

12.

Альпер, Г. А., et al.. (2008). The viscosity of the methanol-n-heptane system at low methanol concentrations. Russian Journal of Physical Chemistry A. 82(1). 68–70. 4 indexed citations

13.

Terekhova, I. V., R. S. Kumeev, & Г. А. Альпер. (2007). The interaction of caffeine with substituted cyclodextrins in water. Russian Journal of Physical Chemistry A. 81(7). 1071–1075. 10 indexed citations

14.

Альпер, Г. А., et al.. (2007). A method for calculating the limiting activity coefficients of nonelectrolytes in mixed solvents based on associated solution theory. Russian Journal of Physical Chemistry A. 81(7). 1088–1091. 1 indexed citations

15.

Golubev, Vladimir V., et al.. (2006). A volumetric investigation of solvophobic effects in halide-n-alkanol-n-alkane ternary systems. Russian Journal of Physical Chemistry A. 80(2). 205–209. 4 indexed citations

16.

Альпер, Г. А., et al.. (2006). The viscosity and density of the methanol + n-nonane, ethanol + n-nonane, and ethanol + n-decane systems. Russian Journal of Physical Chemistry A. 80(10). 1676–1679. 6 indexed citations

17.

Terekhova, I. V., et al.. (2005). Complexation of Amino Acids with 18-Crown-6. Russian Journal of General Chemistry. 75(3). 409–411. 3 indexed citations

18.

Terekhova, I. V., et al.. (2005). 1H NMR study of complexation of α- and β-cyclodextrins with some biologically active acids. Russian Journal of Coordination Chemistry. 31(3). 218–220. 14 indexed citations

19.

Альпер, Г. А., et al.. (2001). Comparative Analysis of the Methods for Calculating the Viscosity of Binary Nonelectrolyte Mixtures. Russian Journal of Applied Chemistry. 74(5). 822–829. 1 indexed citations

20.

Альпер, Г. А., et al.. (1991). Molecular association in mixtures of acetonitrile with amides. Russian Chemical Bulletin. 40(7). 1325–1330. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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