List of publications

Articles, reviews, books (127 publications). [citation data according to WOS and/or Scopus; 2684 total citations, h index = 28; papers with 10+ citations indicated in parenthesis in black; 20+ citations in green; 40+ citations in blue; 60+ citations in red; 80+ citations in magenta; five key articles are marked with asterisk]

127. Hu X., Yin Zh., Guo, J., Borovkov V., Shan Z. An efficient method for long-term configurational stabilization of chiral tricyclic dipeptide via heterocomplexation approach. ChemistrySelect, 2019, 4, 3210-3213.

126. Gawade P.M., Khose V.N., Badani P.M., Hasan M., Kaabel S., Mobin S.M., Borovkov V., Karnik A.V. Benzyne-mediated non-concerted pathway towards synthesis of sterically crowded [5] and [7]-oxahelicenoids, stereochemical and theoretical studies and optical resolution of helicenoids. J. Org. Chem., 2019, 84, 860-868.

125. Mamardashvili G.M., Maltceva O.V., Lazovskiy D.A., Khodov I.A., Borovkov V., Mamardashvili N.Zh., Koifman O.I. Medium viscosity effect on fluorescent properties of Sn(IV)-tetra(4-sulfonatophenyl)porphyrin complexes in buffer solutions. J. Mol. Liquids, 2019, 277, 1047-1053.

124. Bettini S., Pagano R., Borovkov V., Giancane G., Valli L. The role of the central metal ion of ethane-bridged bis-porphyrins in histidine sensing. J. Colloid Interface Sci., 2019, 533, 762-770.

123. Buccolieri A., Hasan M., Bettini S., Bonfrate V., Salvatore L., Santino A., Borovkov V., Giancane G. Ethane-bridged bis-porphyrin conformational changes as an effective analytical tool for non-enzymatic detection of urea in the physiological range. Anal. Chem., 2018, 90, 6952-6958.

122. Osawa T., Wakasugi M., Kizawa T., Borovkov V., Inoue Y. Enantio-differentiating hydrogenation of alkyl 3-oxobutanoates over tartaric acid-modified Ni catalyst: enthalpy-entropy compensation effect as a tool for elucidating mechanistic features. Mol. Catal., 2018, 449, 131-136.

121. Buccolieri A., Manno D., Serra A., Santino A., Hasan M., Borovkov V., Giancane G. Highly sensitive conformational switching of ethane-bridged mono-zinc bis-porphyrin as an application tool for rapid monitoring of aqueous ammonia and acetone. Sensor Actuat. B-Chem., 2018, 257, 685-691.

120. Maljutenko K., Borovkov V., Kananovich D. J?rving I., Lopp M. Aerobic cascade oxidation of substituted cyclopentane-1,2-diones using metalloporphyrin catalysts. Tetrahedron, 2018, 74, 661-664.

119. Khose V.N., John M.E., Pandey A.D., Borovkov V., Karnik A.V. Chiral heterocycle base receptors for enantioselective recognition. Symmetry, 2018, 10, 34. (invited review, featured paper in 2018)

118. Hasan M., Borovkov V. Helicene-based chiral auxiliaries and chirogenesis. Symmetry, 2018, 10, 10. (invited review, featured paper in 2018, selected cover picture)

117. Borovkov V. Supramolecular chirogenesis and chirality sensing. Arch. Chem. Res. (Proceedings of 8th Edition of International Conference on Chemical Science, London, UK, June 14-15, 2018), 2018, 2, 66.

116. Borovkov V. Chirogenesis in supramolecular systems on the basis of porphyrinoids. Proceedings, 2018, 2, 67.

115. Konrad N., Kananovich D., Aav R., Borovkov V. Spectroscopic study of (all-R,R)-cyclohexanohemicucurbit[8]uril and its host-guest supramolecular hexafluorophosphate complexes. Proceedings, 2018, 2, 64.

114. Elek G.Z., Borovkov V., Lopp M., Kananovich D.G. Enantioselective one-pot synthesis of α,β-epoxy ketones via aerobic oxidation of cyclopropanols. Org. Lett., 2017, 19, 3544-3547.

113. Colombelli A., Manera M.G., Borovkov V., Giancane G., Valli L., Rella R. Enhanced sensing properties of cobalt bis-porphyrin derivative thin films by a magneto-plasmonic-opto-chemical sensor. Sensor Actuat. B-Chem., 2017, 246, 1039-1048.

112. Hasan M., Khose V.N., Mori T., Borovkov V., Karnik A.V. Sui generis helicene-based supramolecular chirogenic system: enantioselective sensing, solvent control, and application in chiral group transfer reaction. ACS Omega, 2017, 2, 592-598.

111. Borovkov V., Gathergood N. Porphyrinoids based supramolecular probes for chirality sensing. Symmetry: Culture and Science, 2017, 28, 175-178.

110. Borovkov V., Gathergood N.  Symmetry and asymmetry phenomena in chemical, green, and related sciences. Symmetry: Culture and Science, 2017, 28, 165-166. (editorial)

109. Hasan M., Khose V.N., Pandey A.D., Borovkov V., Karnik A.V. Tailor-made supramolecular chirogenic system based on C_s?symmetric rigid organophosphoric acid host and amino alcohols: mechanistic studies, bulkiness effect, and chirality sensing. Org. Lett., 2016, 18, 440-443.

108. Bettini S., Maglie E., Pagano R., Borovkov V., Inoue Y., Valli L, Giancane G. Conformational switching of an ethano-bridged Cu,H₂-bis-porphyrin induced by aromatic amines. Beilstein J. Nanotechnol. 2015, 6, 2154-2160.

107. Borovkov V. Book Review of “Lanthanide Metal-Organic Frameworks”. Front. Chem., 2015, 3, 50, doi: 10.3389/fchem.2015.00050. (invited review)

106. Osawa T., Kizawa T., Ikeda S., Kitamura T., Inoue Y., Borovkov V. Enhanced enantioselectivity in heterogeneous catalytic hydrogenation of acetoacetate esters to corresponding 3-hydroxybutyrates using commercial nickel powder. Tetrahedron: Asymmetry, 2014, 25, 1630-1633.

105. Borovkov V., Rein R., Solladié N. Spatial organization of multi-porphyrinoids for pre-defined properties. In Handbook of Porphyrin Science; Eds. Kadish K.M., Smith K.M., Guilard R.; World Scientific Publishing: Singapore, 2014, Vol. 32, pp 368-428. (invited chapter)

104. Borovkov V. Supramolecular chirality in porphyrin chemistry. Symmetry, 2014, 6, 256-294. (invited review, featured paper in 2014, Editors’ Choice) [28]

103. Borovkov V. Supramolecular chirality sensing and enantioselective catalysis. Symmetry: Culture and Science, 2014, 25, 55-58.

102. Borovkov V., Petitjean M. Chirality and symmetry in the chemical and physical structure of matter. Symmetry: Culture and Science, 2014, 25, 53-54. (editorial)

101. Osawa T., Kizawa T., Takano F., Ikeda S., Kitamura T., Inoue Y., Borovkov V. Catalytic enantiodifferentiating hydrogenation with commercial nickel powders chirally modified by tartaric acid and sodium bromide. ChemCatChem, 2014, 6, 170-178.

100. Osawa T., Kizawa T., Ikeda S., Kitamura T., Inoue Y., Borovkov V. Heterogeneous enantioselective hydrogenation: pH dependence and interplay between catalytic efficacy and surface composition. Chem. Lett., 2013, 42, 1225-1226.

99. Borovkov V. From supramolecular chirogenic systems towards prospective functional materials. Advanced Materials Research, 2013, 699, 87-91.

98. Giancane G., Borovkov V., Inoue Y., Conoci S., Valli L. Syn-anti conformation switching of a bis-porphyrin derivative at the air-water interface and in the solid state as an effective tool for chemical sensing. Soft Matter, 2013, 9, 2301-2307. [19]

97. Osawa T., Lee I-Y.S., Ikeda S., Kitamura T., Inoue Y., Borovkov V. Simplified preparation of chirally modified nickel catalyst for enantioselective hydrogenation: a step forward to industrial use. Appl. Catal. A-Gen., 2012, 445-446, 269-273. [12]

96. Giancane G., Borovkov V., Inoue Y., Valli L. Conformational switching in bis(zinc porphyrin) Langmuir-Schaefer film as an effective tool for selectively sensing aromatic amines. J. Colloid Interface Sci., 2012, 385, 282-284. [12]

95. Mandal S., Bhattacharyya S., Borovkov V., Patra A. Photophysical properties, self-assembly behavior, and energy transfer of porphyrin-based functional nanoparticles. J. Phys. Chem. C, 2012, 116, 11401-11407. [37]

94. Osawa T., Borovkov V. Application of chirally modified nickel catalysts for production of optically active compounds. Recent Patents on Catalysis, 2012, 1, 27-34. (invited review)

93. Mandal S., Bhattacharyya S., Borovkov V., Patra A. Porphyrin-based functional nanoparticles: conformational and photophysical properties of bis-porphyrin and bis-porphyrin encapsulated polymer nanoparticles. J. Phys. Chem. C, 2011, 115, 24029–24036. [18]

92. Osawa T., Kizawa T., Lee I-Y.S., Ikeda S., Kitamura T., Inoue Y., Borovkov V. Durability enhancement of chirally modified metallic nickel catalysts for enantioselective hydrogenation. Catal. Commun., 2011, 15, 15-17. [10]

91. Borovkov V., Osawa T. From supramolecular chirogenesis towards functional chiral material. Oggi Chim./Chem. Today, 2011, 29, n. 5, 28-30. (invited review)

90. Borovkov V. Effective Supramolecular chirogenesis in ethane-bridged bis-porphyrinoids. Symmetry, 2010, 2, 184-200. (invited review)

89. Borovkov V., Inoue Y. A versatile bisporphyrinoid motif for supramolecular chirogenesis. Eur. J. Org. Chem., 2009, 189-197. (invited review, selected cover picture) [12]

88. Schnatwinkel B., Rekharsky M.V., Brodbeck R., Borovkov V.V., Inoue Y., Mattay J. Thermodynamic aspects of the host-guest chemistry of pyrogallol[4]arenas and peralkylated ammonium cations. Tetrahedron, 2009, 65, 2711-2715.

87. Schnatwinkel B., Rekharsky M.V., Borovkov V.V., Inoue Y., Mattay J. Pyrogallol[4]arenas as artificial receptors for L-carnitine. Tetrahedron Lett., 2009, 50, 1374-1376. [16]

86. Mamardashvili N.Zh., Borovkov V.V., Mamardashvili G.M., Inoue, Y., Koifman O.I. Complexation of porphyrins with ions and organic molecules. In Chemical Processes with Participation of Biological and Related Compounds. Biophysical and Chemical Aspects of Porphyrins, Pigments, Drugs, Biodegradable Polymers and Nanofibers; Eds. Lomova T.N., Zaikov G.E.; Koninklijke Brill: Leiden, 2008, pp 117-168. (invited chapter)

85. Schnatwinkel B., Stoll I., Mix A., Rekharsky M.V., Borovkov V.V., Inoue Y., Mattay J. Monomeric, dimeric and hexameric recorcin[4]arene assemblies with alcohols in apolar solvents. Chem. Commun., 2008, 3873-3875. [32]

84. Borovkov V., Yamamoto T., Higuchi H., Inoue Y. Supramolecular chirogenesis in weakly interacting hosts: role of the temperature, structural and electronic factors in enhancement of chiroptical sensitivity. Org. Lett., 2008, 10, 1283-1286. [13]

*83. Hembury G.A., Borovkov V.V., Inoue Y. Chirality sensing supramolecular systems. Chem. Rev., 2008, 108, 1-73. (invited review, a Most-Accessed Article for the first-quarter of 2008) [604]

82. Bhyrappa P., Borovkov V.V., Inoue Y. Supramolecular chirogenesis in bis-porphyrins: interaction with chiral acids and application for the absolute configuration assignment. Org. Lett., 2007, 9, 433-435. [29]

81. Borovkov V.V., Mamardashvili N. Zh., Inoue Y. Optically active supramolecular systems on the basis of porphyrins. Russ. Chem. Rev., 2006, 75, 820-832. (review) [13]

80. Borovkov V.V., Inoue Y. Supramolecular chiral recognition by bischlorins: a two-point interaction mode combined with the host’s conformational modulation controlled by the guest’s stereochemistry and bulkiness. Org. Lett., 2006, 8, 2337-2340. [18]

79. Borovkov V.V., Inoue Y. Supramolecular chirogenesis in host-guest systems containing porphyrinoids. Top. Curr. Chem., 2006, 265, 89-146. (invited review) [35]

78. Fujii I, Borovkov V.V., Inoue Y. Crystal structure of bis-Zn-porphyrin. Anal. Sci., 2006, 22, x77-x78.

77. Hodgson M.J., Borovkov V.V., Inoue Y., Arnold D.P. A new type of chiral porphyrin: organopalladium porphyrins with chiral chelating diphosphine ligands. J. Organomet. Chem., 2006, 691, 2162-2170. [20]

76. Valli L., Casilli S., Giotta L., Pignataro B., Conoci S., Borovkov V.V., Inoue Y., Sortino S. Ethane-bridged zinc-porphyrin dimers in Langmuir-Sh?fer thin films: structural and spectroscopic properties. J. Phys. Chem. B, 2006, 110, 4691-4698. [23]

75. Scheil C., Hembury G.A., Borovkov V.V., Klaes M., Agena C., Wada T., Grimme S., Inoue Y., Mattay J. New insights into the geometry of resorc[4]arenes: solvent-mediated supramolecular conformational and chiroptical control. J. Org. Chem., 2006, 71, 976-982. [28]

74. Borovkov V.V., Hembury G. A., Inoue Y. Supramolecular chirogenesis with bis-chlorin versus bis-porphyrin hosts: peculiarities of chirality induction and modulation of optical activity. J. Org. Chem., 2005, 70, 8743-8754. [23]

73. Borovkov V.V., Muranaka A., Hembury G. A., Origane Y., Ponomarev G. V., Kobayashi N., Inoue Y. Chiral bis-chlorin: effective enantiomer resolution and absolute configuration determination. Org. Lett., 2005, 7, 1015-1018. [21]

72. Borovkov V.V., Fujii I., Muranaka A., Hembury G.A., Tanaka T., Ceulemans A., Kobayashi N., Inoue Y. Rationalization of supramolecular chirality in a bisporphyrin system. Angew. Chem. Int. Ed., 2004, 43, 5481-5485. [66]

71. Borovkov V.V., Casilli S., Conoci S., Inoue Y., Sortino S., Valli L. Molecular organization and syn-anti conformational equilibria in ethane-bridged bis(zinc porphyrin) floating films at the air-water interface. Surf. Sci., 2004, 572, 66-76.

*70. Borovkov V.V., Hembury G.A., Inoue Y. Origin, control, and application of supramolecular chirogenesis in bis-porphyrin-based systems. Acc. Chem. Res., 2004, 37, 449-459. (invited review) [149]

*69. Borovkov V.V., Hembury G.A., Inoue Y. The origin of solvent-controlled supramolecular chirality switching in a bis(zinc porphyrin) system. Angew. Chem. Int. Ed., 2003, 42, 5310-5314. [68]

68. Borovkov V.V., Hembury G.A., Yamamoto N., Inoue Y. Supramolecular chirogenesis in zinc porphyrins: investigation of zinc-freebase bis-porphyrin, new mechanistic insights, extension of sensing abilities and solvent effect. J. Phys. Chem. A, 2003, 107, 8677 - 8686. [33]

67. Borovkov V.V., Lintuluoto J.M., Hembury G.A., Sugiura M., Arakawa R., Inoue Y. Supramolecular chirogenesis in zinc porphyrins: interaction with bidentate ligands, formation of tweezer structures, and the origin of enhanced optical activity. J. Org. Chem., 2003, 68, 7176-7192. [51]

66. Borovkov V.V., Hembury G.A., Inoue Y. Enthalpy-entropy compensation upon syn-anti conformational switching of bis-porphyrins by amines and alcohols. J. Porphyrins Phthalocyanines, 2003, 7, 337-341.

65. Hembury G.A., Borovkov V.V., Lintuluoto J.M., Inoue Y. An acid–base controlled molecular switch. syn–anti conformational switching in a μ-oxo bis(iron porphyrin). Chem. Lett., 2003, 32, 428-429. [13]

64. Borovkov V.V., Harada T., Hembury G.A., Inoue Y., Kuroda R. Solid state supramolecular chirogenesis: high optical activity and gradual development of zinc octaethylporphyrin aggregates. Angew. Chem. Int. Ed., 2003, 42, 1746-1749. [42]

63. Lintuluoto J.M., Borovkov V.V., Hembury G.A., Inoue Y. Spectroelectrochemistry of porphyrin containing mono- and hetero-bimetallic systems: porphyrin-Ru(bpy)₃ conjugates. Bull. Chem. Soc. Jpn., 2003, 76, 309-316.

62. Panzera, G., Conoci, S., Coffa, S., Pignataro, B., Sortino, S., Valli, L., Borovkov, V.V., Inoue, Y. Structural and spectroscopic study of Langmuir-Sch?fer films of bis Zn-ethane-bridged porphyrins dimer. Materials Research Society Symposium – Proceedings, 2003, 771, 255-259.

61. Lintuluoto J.M., Borovkov V.V., Inoue Y. Direct determination of absolute configuration of monoalcohols by bis(magnesium porphyrin). J. Am. Chem. Soc., 2002, 124, 13676-13677. [56]

60. Borovkov V.V., Lintuluoto J.M., Sugiura M., Inoue Y., Kuroda R. Remarkable stability and enhanced optical activity of a chiral supramolecular bis-porphyrin tweezer in both solution and solid state. J. Am. Chem. Soc., 2002, 124, 11282-11283. [46]

59. Borovkov V.V., Harada T., Inoue Y., Kuroda R. Phase-sensitive supramolecular chirogenesis in bis-porphyrin systems. Angew. Chem. Int. Ed., 2002, 41, 1378-1381. (VIP) [46]

58. Borovkov V.V., Lintuluoto J.M., Sugeta H., Fujiki M., Arakawa R., Inoue Y. Supramolecular chirogenesis in zinc porphyrins: equilibria, binding properties, and thermodynamics. J. Am. Chem. Soc., 2002, 124, 2993-3006. [66]

57. Borovkov V.V., Lintuluoto J.M., Inoue Y. Stoichiometry-controlled supramolecular chirality induction and inversion in bis-porphyrin systems. Org. Lett., 2002, 4, 169-171. [45]

56. Hesek D., Hembury G.A., Drew M.G.B., Borovkov V.V., Inoue Y. Photochromic atropisomer generation and conformation determination in a ruthenium bis(bipyridine) phosphonite g-cyclodextrin system. J. Am. Chem. Soc., 2001, 123, 12232-12237. [16]

55. Borovkov V.V., Lintuluoto J.M., Inoue Y. Roles of guest structure and external factors in controlling supramolecular chirogenesis in bis-porphyrin host. Polym. Prep. Jpn., 2001, 50, 1552-1553.

54. Borovkov V.V., Yamamoto N., Lintuluoto J.M., Tanaka T., Inoue Y. Supramolecular chirality induction in bis(zinc porphyrin) by amino acid derivatives: rationalization and applications of the ligand bulkiness effect. Chirality, 2001, 13, 329-335. (Dedicated to Prof. K Nakanishi) [44]

*53. Borovkov V.V., Lintuluoto J.M., Inoue Y. Supramolecular chirogenesis in zinc porphyrins: mechanism, role of guest structure, and application for the absolute configuration determination. J. Am. Chem. Soc., 2001, 123, 2979-2989. [145]

52. Borovkov V.V., Inoue Y. Bis(zinc porphyrin) as reagent for determination of the absolute configuration of chiral compounds. Wako Chemical Reports, 2001, 69, 31-33 (Jpn).

51. Borovkov V.V., Lintuluoto J.M., Inoue Y. Elucidation of the mechanism of supramolecular chirality inversion in bis(zinc porphyrin) by dynamic approach using CD and ¹H NMR spectroscopy. J. Phys. Chem. A, 2000, 104, 9213-9219. [29]

50. Lintuluoto J.M., Borovkov V.V., Inoue Y. Synthesis and fluorescence behavior of novel Ru(bpy)3-porphyrin conjugates. Tetrahedron Lett., 2000, 41, 4781-4786. [14]

49. Borovkov V.V., Lintuluoto J.M., Inoue Y. Supramolecular chirogenesis in bis(zinc porphyrin): an absolute configuration probe highly sensitive to guest structure. Org. Lett., 2000, 2, 1565-1568. [57]

*48. Borovkov V.V., Lintuluoto J.M., Fujiki M., Inoue Y. Temperature effect on supramolecular chirality induction in bis(zinc porphyrin). J. Am. Chem. Soc., 2000, 122, 4403-4407. [96]

47. Borovkov V.V., Lintuluoto J.M., Inoue Y. Syn-anti conformational changes in zinc porphyrin dimers induced by temperature-controlled alcohol ligation. J. Phys. Chem. B, 1999, 103, 5151-5156. [50]

46. Borovkov V.V., Lintuluoto J.M., Inoue Y. Temperature controlled syn-anti conformational switching in zinc containing porphyrin dimers via ligand assistance. Tetrahedron Lett., 1999, 40, 5051-5054. [23]

45. Borovkov V.V., Lintuluoto J.M., Inoue Y. Synthesis of Zn-, Mn, and Fe-containing mono- and heterometallated ethanediyl-bridged porphyrin dimers. Helv. Chim. Acta, 1999, 82, 919-934. [46]

44. Borovkov V.V., Lintuluoto J.M., Inoue Y. Convenient method for efficient iron and manganese ion insertion into various porphyrins under mild conditions. Synlett, 1999, 61-62. [21]

43. Cheremenskaya O.V., Solov''''''''''''''''''''''''''''''''eva A.B., Borovkov V.V., Ponomarev G.V., Yashunskii D.V., Timashev S.F. Kinetics of hydroxylation of cholesterol in the presence of the ethane-bridged Mn-Cu-bis(etioporphyrinate) heterodimer. Russ. J. Phys. Chem., 1999, 73, 2262-2264 (Russ.).

42. Borovkov V.V., Lintuluoto J.M., Inoue Y. Efficient synthesis of unsymmetrical transition metalloporphyrin dimers under mild conditions. Synlett, 1998, 768-770. [13]

41. Solov''''''''''''''''''''''''''''''''eva A.B., Cheremenskaya O.V., Borovkov V.V., Ponomarev G.V., Timashev S.F. Kinetic patterns of hydroxylation of cholesterol in the presence of dimeric manganese porphyrinates. Russ. J. Phys. Chem., 1998, 72, 1601-1606 (Russ.).

40. Ponomarev G.V., Yashunsky D.V., Borovkov V.V., Sakata Y., Arnold D. Porphyrins. 36. Cis-trans- and atropisomerism in molecules of ethylenebisporphyrins. Russ. Chem. Heterocycl. Comp., 1997, 1627-1645 (Russ.).

39. Borovkov V.V., Solovieva A.B., Cheremenskaya O.V., Belkina N.V. Enhancement of catalytic efficiency of metalloporphyrin-reductant-molecular oxygen biomimetic system by amino acid external ligands. J. Mol. Catal. A: Chem., 1997, 120, L1-L4.

38. Solovieva A.B., Cheremenskaya O.V., Belkina N.V., Evstigneeva R.P., Zheltukhina G.A., Borovkov V.V. The effect of amino acids on the rate of hydroxylation of cholesterol catalyzed by Mn and Fe porphyrinates. Russ. Chem. Bull., 1996, 3000-3003 (Russ.).

37. Fujii A., Zakhidov A.A., Borovkov V.V., Ohmori Y., Yoshino K. Organic photovoltaic cell with donor-acceptor double heterojunctions. Jpn. J. Appl. Phys., 1996, 35, L1438-L1441. [24]

36. Arnold D.P., Borovkov V.V., Ponomarev G.V. Redox-induced cis —> trans isomerisation of bis(porphyrinyl)ethenes: a possible basis for a molecular memory element? Chem. Lett., 1996, 485-486. [33]

35. Borovkov V.V., Anikin M., Wasa K., Sakata Y. Structurally controlled porphyrin-aggregation process in phospholipid membranes. Photochem. Photobiol., 1996, 63, 477-482. [17]

34. Borovkov V.V., Evstigneeva R.P., Gribkov A.A. Synthesis of triad molecular-system containing covalently-linked photosensitizer, mesoporphyrin II, secondary electron donor and acceptor, for modeling process of photosynthesis. Russ. Chem. Heterocycl. Comp., 1995, 343-350 (Russ.).

33. Solovieva A.B., Borovkov V.V., Lukashova E.A., Grinenko G.S. High efficient catalytic oxidation of steroidal olefins by metalloporphyrin-reductant-molecular oxygen biomimetic systems. Chem. Lett., 1995, 441-442.

32. Kiryuhin Yu.I., Solovieva A.B., Lukashova E.A., Korol''''''''''''''''''''''''''''''''kova M.L., Belkina N.V., Ponomarev G.V., Borovkov V.V. Characteristics of photooxidation of anthracene sensibilized with manganese porphyrinates. Russ. J. Phys. Chem., 1995, 69, 922-925 (Russ.).

31. Stolovitsky Y.M., Kiselev B.A., Suponeva E.P., Paschenko V.Z., Tusov V. B., Vasiliev S.E., Alimova E.V., Sadovnikova N.A., Olovyanishnikova G. D., Borovkov V.V., Filippovich E.I., Luzgina V.N., Evstigneeva R.P. Investigation of the energetics of covalently bound molecular systems of deuteroporphyrin IX with quinone derivatives. Russ. Biophysics, 1995, 40, 19-22 (Russ.). [25]

30. Ponomarev G.V., Borovkov V.V., Shul''''''''''''''''''''''''''''''''ga A.M., Sakata Y. Cis-trans isomerisation and atropisomerism of octaethyl 1,2-bis(coproporphyrinyl)ethylene ester. J. Chem. Soc., Chem. Commun., 1994, 1927-1928. [21]

29. Anikin M.V., Borovkov V.V., Ishida A., Wasa K., Sakata Y. Observation of conformational relaxation hindrance in the singlet excited state for porphyrin incorporated in a lipid membrane. Chem. Phys. Lett., 1994, 226, 337-343.

28. Gribkov A.A., Borovkov V.V., Evstigneeva R.P., Sakata Y. Synthesis of rigid triads based on octaalkylporphyrin, capable to multistep electron transfer. Russ. Chem. Heterocycl. Comp., 1994, 1052-1062 (Russ.).

27. Zaliznaya N.F., Borovkov V.V., Davydov B.E., Mavrenkova G.V., Karpacheva G.P., Kryukov A.Yu., Khailova E.B. Preparation and properties of porphyrin-containing polymers. Polymer Science, 1993, 35, 15-17.

26. Borovkov V.V., Ponomarev G.V., Ishida A., Kaneda T., Sakata Y. Mechanistic studies on oxidation reaction of ethane-bridged porphyrin dimers to trans-ethylene-bridged species. Chem. Lett., 1993, 1409-1412. [23]

25. Kitagawa R., Kai Y., Ponomarev G.V., Sugiura K., Borovkov V.V., Kaneda T., Sakata Y. Highly crowded trans-olefin. Molecular structure of trans-1,2-bis{meso-[nickel(II)octaethylporphyrinyl]}ethene. Chem. Lett., 1993, 1071-1074. [29]

24. Ponomarev G.V., Borovkov V.V., Sugiura K., Sakata Y., Shul''''''''''''''''''''''''''''''''ga A.M. Synthesis and properties of cis-1,2-bis(octaethylporphyrinyl)ethylene. Tetrahedron Lett., 1993, 34, 2153-2156. [71]

23. Borovkov V.V., Ishida A., Takamuku S., Sakata Y. A new approach to study of solvent effect on intramolecular electron transfer. Chem. Lett., 1993, 737-740.

22. Borovkov V.V., Ishida A., Takamuku S., Sakata Y. Evidence for parallel photoinduced electron transfer in diquinone substituted porphyrins. Chem. Lett., 1993, 145-148.

21. Katz E.Y., Borovkov V.V., Evstigneeva R.P. Application of quinone thio derivatives as a basis for assembling complex molecular systems at an electrode surface. J. Electroanal. Chem., 1992, 326, 197-212. [31]

20. Borovkov V.V., Sakata Y., Ishida A. Study of electron-transfer process in photosynthetic model compounds by single photon counting method. Radiation Lab. Lett. (ISIR, Osaka Univ.), 1992, 9, 5-7 (Jpn.).

19. Borovkov V.V., Gribkov A.A., Sakata Y. Synthesis and photochemical studies of triadic photosynthetic model. In Research in Photosynthesis (Proceedings of the 9th International Congress on Photosynthesis, Nagoya, Japan, August 30-September 4, 1992); Ed. Murata N.; Kluwer Academic Publishers: Dordrecht, 1992, Vol. 2, pp 841-844.

18. Borovkov V.V., Gribkov A.A., Kozyrev A.N., Brandis A.S., Ishida A., Sakata Y. Synthesis and properties of pheophorbide-quinone compounds. Bull. Chem. Soc. Jpn., 1992, 65, 1533-1537. [15]

17. Borovkov V.V., Evstigneeva R.P., Makova S.Z. Synthesis of deuteroporphyrin IX diquinone derivatives for the studies of primary photosynthetic stages. Russ. Chem. Heterocycl. Comp., 1992, 176-182 (Russ.).

16. Katz E.Y., Borovkov V.V., Evstigneeva R.P. Use of thio derivatives of quinones for the chemical modification of electrodes. Sov. Electrochem., 1991, 27, 1035-1041 (Russ.).

15. Borovkov V.V., Evstigneeva R.P., Mirakova E.V., Rozynov B.V. Synthesis of the capped photosynthetic model system based on mesoporphyrin II. Russ. Chem. Heterocycl. Comp., 1991, 1419-1423 (Russ.).

14. Borovkov V.V., Gribkov A.A., Evstigneeva R.P., Struganova I.A., Ponomarev G.V., Kirillova G.V., Rozynov B.V., Bondarenko P.V., Zuborev R.A., Knysh A.N. Synthesis and spectroscopic studies of the hematoporphyrin IX diquinone derivatives. Russ. Chem. Heterocycl. Comp., 1991, 1324-1330 (Russ.).

13. Borovkov V.V., Evstigneeva R.P., Kirillova G.V., Ponomarev G.V., Rozynov B.V. Synthesis of a photosynthetic donor-acceptor system containing covalently linked amine, porphyrin and quinone. Russ. Chem. Heterocycl. Comp., 1991, 196-199 (Russ.).

12. Borovkov V.V., Evstigneeva R.P., Kamalov V.F., Struganova I.A., Toleutaev B.N. Mechanism of charge transfer in the molecular DPQ complex studied by time-resolved fluorescence spectroscopy. J. Phys. Chem., 1991, 95, 6437-6440.

11. Borovkov V.V., Evstigneeva R.P., Kitaigorodsky A.N., Chamaeva O.A., Chupin V.V. ¹H-NMR study of conformational equilibrium in porphyrin-quinones with a flexible covalent bridge between chromophores. Proc. USSR Acad. Sci., 1990, 312, 382-386 (Russ.).

10. Borovkov V.V., Evstigneeva R.P., Kamalov V.F., Struganova I.A., Toleutaev B.N. Dynamics of charge separation in a dimethylaniline-mesoporphyrin II-quinone model photosynthetic system. Russ. Opt. Spectr., 1990, 68, 81-87 (Russ.).

9. Borovkov V.V., Evstigneeva R.P. Synthesis of photosynthetic models based on porphyrin-quinone compounds. In Proceedings of the F.E.C.S. 5th International Conference on Chemistry and Biotechnology of Biologically Active Natural Products, Varna, Bulgaria; 1989, Vol. 3, pp 412-413.

8. Borovkov V.V., Evstigneeva R.P., Filippovich E.I., Rozynov B.V. Synthesis of donor-acceptor molecules based on mesoporphyrin II capable to photoinduced electron transfer. Proc. USSR Acad. Sci., 1989, 308, 874-878 (Russ.).

7. Borovkov V.V., Evstigneeva R.P., Strekova L.N., Filippovich E.I. Porphyrin-quinone compounds as synthetic models of the reaction centre in photosynthesis. Russ. Chem. Rev., 1989, 58, 602-619 (review). [21]

6. Struganova I.A., Borovkov V.V., Evstigneeva R.P. Picosecond stages of the electron transfer in the molecular DPQ complex studied by time-resolved fluorescence spectroscopy. In Proceedings of the 6th International Conference on Energy and Electron Transfer, Prague, Czechoslovakia; Eds. Fiala and Pokorny; 1989, Vol. 1. p 70.

5. Borovkov V.V., Kamalov V.F., Struganova I.A., Toleutaev B.N., Evstigneeva R.P. Dynamics of the first charge separation step in the dimethylaniline-mesoporphyrin-quinone triad. Proc. USSR Acad. Sci., 1989, 305, 223-226 (Russ.).

4. Khairutdinov R.F., Strekova L.N., Borovkov V.V., Filippovich E.I., Evstigneeva R.P. Low temperature photo and dark electron transfer reactions in glass solutions of the porphyrin-quinone compounds. Russ. Chem. High Energy, 1988, 22, 520-525 (Russ.).

3. Borovkov V.V., Filippovich E.I., Evstigneeva R.P. Synthesis and studies of spectral properties of the porphyrin-quinone derivatives based on deuteroporphyrin IX. Russ. Chem. Heterocycl. Comp., 1988, 608-616 (Russ.). [19]

2. Strekova L.N., Borovkov V.V., Filippovich E.I., Khairutdinov R.F., Evstigneeva R.P. Modelling of the intermediate step of the primary photosynthetic charge separation by porphyrin-quinone compounds. Proc. USSR Acad. Sci., 1988, 298, 487-491 (Russ.).

1. Evstigneeva R.P., Borovkov V.V., Filippovich E.I., Sviridov S.I. Synthesis of the diquinone derivatives of porphyrins. Proc. USSR Acad. Sci., 1987, 293, 1130-1132 (Russ.). [13]