Dr. Helena Dodziuk
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Dr. Helena Dodziuk

Medical Professional/Doctor
Polish Academy of Sciences, Poland

Highest Degree
Ph.D. in Pharmacology from Polish Academy of Sciences, Poland

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Area of Interest:

Pharmacology and Toxicology
100%
Cancer Pharmacology
62%
Drug Discovery
90%
Inflammation
75%
Immunopharmacology
55%

Research Publications in Numbers

Books
0
Chapters
0
Articles
0
Abstracts
0

Selected Publications

  1. Dodziuk, H., V. Vetokhina, H. Hopf, R. Luboradzki, P. Gawel and J. Waluk, 2012. Electronic states of cyclophanes with small bridges. J. Chem. Phys., Vol. 136, No. 7. 10.1063/1.3683454.
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  2. Korona, T. and H. Dodziuk, 2011. Small molecules in C60 and C70: Which complexes could be stabilized? J. Chem. Theor. Comput., 7: 1476-1483.
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  3. Dodziuk, H., S. Szymanski, J. Jazwinski, M. Ostrowski and T. Demissie et al., 2011. Structure and NMR spectra of some [2.2]paracyclophanes. The dilemma of [2.2]paracyclophane symmetry. J. Phys. Chem. A, 115: 10638-10649.
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  4. Dodziuk, H., A. Bielejewska, W. Schilf and H. Ueda, 2011. Complexation of [2.2]paracyclophane with β- and γ-cyclodextrins studied by HPLC and NMR. Cent. Eur. J. Chem., 9: 1056-1061.
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  5. Dodziuk, H., S. Szymanski, J. Jazwinski, M.E. Marchwiany and H. Hopf, 2010. Structure and dynamics of [3.3]paracyclophane as studied by nuclear magnetic resonance and density functional theory calculations. J. Phys. Chem. A, 114: 10467-10473.
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  6. Dodziuk, H., M. Ostrowski and M.E. Marchwiany, 2010. NMR parameters of two tricyclododecadienes-strained hydrocarbons with close distance between perpendicularly or parallel arranged double bonds. Magn. Res. Chem., 48: 173-178.
    PubMed  |  
  7. Dodziuk, H. and M. Pietrzak, 2010. CPMAS study of rings inversion of cis-decalin in the solid state when complexed with-cyclodextrin. Austr. J. Chem., 63: 709-711.
  8. Bernatowicz, P., A. Ejchart, K. Ruszczynska-Bartnik, H. Dodziuk, E. Kaczorowska-Molchanow and H. Ueda, 2010. Carbon-13 NMR relaxation study of the internal dynamics in cyclodextrins in isotropic solution. J. Phys. Chem. B., 114: 59-65.
  9. Korona, T., M. Hesselmann and H. Dodziuk, 2009. Symmetry-adapted perturbation theory applied to endohedral fullerene complexes: A stability study of H2@C60 and2H2@C60. J. Chem. Theory Comput., 5: 1585-1596.
  10. Dodziuk, H., M. Ostrowski, K. Ruud, J. Jazwinski, H. Hopf and W. Kozminski, 2009. Spatial structure and NMR spectra of strained [2.2.2] cyclophanes. Magn. Res. Chem., 47: 407-414.
    PubMed  |  
  11. Dodziuk, H., 2007. Modeling the structure of fulleranes and their endohedral complexes involving small molecules with nontrivial topological properties. J. Nanosci. Nanotechnol., 7: 1102-1110.
    PubMed  |  
  12. Dinadayalane, T.C., L. Gorb, T. Simeon and H. Dodziuk, 2007. Cumulative pi-pi interaction triggers unusually high stabilization of linear hydrocarbon inside the single-walled carbon nanotube. Int. J. Quantum. Chem., 107: 2204-2210.
  13. Dodziuk, H. and M. Ostrowski, 2006. The planarization of the cyclohexane ring by building it into a cyclophane cage: Hexahydrosuperphane. Eur. J. Org. Chem., 1: 5231-5237.
  14. Bernatowicz, P., M. Nowakowski, H. Dodziuk and A. Ejchart, 2006. Determination of association constants at moderately fast chemical exchange. Complexation of camphor enantiomers by cyclodextrin. J. Magn. Res., 181: 304-309.
  15. Dodziuk, H., M. Jaszunski and W. Schilf, 2005. 1H and 13C NMR chemical shifts and spin-spin coupling constants in trans- and cis-decalins. Magn. Reson. Chem., 43: 639-646.
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  16. Dodziuk, H., 2005. Reply to the comment on Modelling complexes of H2 molecules in fullerenes. Chem. Phys. Lett., 410: 39-41.
  17. Dodziuk, H., 2005. Modeling complexes of H2 molecules in fullerenes. Chem. Phys. Lett., 410: 39-41.
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  18. Dinadayalane, T.C., L. Gorb, H. Dodziuk and J. Leszczynski, 2005. Modelling of the stabilization of the system consisting of a single walled (5.5) carbon nanotube C60H20 with cumulenic or acetylenic chain. AIP Conf. Proc., 786: 436-439.
  19. Dodziuk, H., W. Kozminski and A. Ejchart, 2004. NMR studies of chiral recognition by cyclodextrins. Chirality, 16: 90-105.
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  20. Dodziuk, H., O.M. Demchuk, W. Schilf and G. Dolgonos, 2004. Synthesis and NMR study of first generation dendrimer having four branches involving four glycine and one carbomoyl-(3,7-dimethoxy-2-naphthalene) groups and unsuccessful attempts to complex it with α-, β- or γ-cyclodextrins. J. Mol. Struct., 693: 1145-1151.
  21. Dodziuk, H., O.M. Demchuk, A. Bielejewska, W. Kozminski and G. Dolgonos, 2004. Chromatographic, NMR and Molecular Modeling Study of Multiple Complexation of α-, β- and γ-cyclodextrins with first generation dendrimer having three branches involving four glycine and one adamantyl groups. Supramol. Chem., 16: 287-292.
  22. Dodziuk, H., O. Demchuk, W. Kozminski and G. Dolgonos, 2003. 1:3 Complex between b-cyclodextrin and dendrimer with three branches involving four glycine and one adamantyl group. Pol. J. Chem., 77: 333-340.
  23. Dodziuk, H., K.S. Nowinski, W. Kozminski and G. Dolgonos, 2003. On the impossibility of determination of stepwise binding constants for the 1: 2 complex of (+)-camphor with α -cyclodextrin. Org. Biomol. Chem., 1: 581-584.
    PubMed  |  
  24. Dodziuk, H., G. Dolgonos and J. Leszczynski, 2003. Tricyclo[2.2.0.01,3]hexane: A new hypothetical molecule which should have only one inverted carbon atom. Tetrahedron, 59: 10013-10018.
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  25. Dodziuk, H., G. Dolgonos and J. Leszczynski, 2003. A quantum chemical study of tricyclo[3.2.0.01,3]heptane: a new hypothetical molecule with unusual spatial structure. Similarities and differences with synand anti-tricyclo[3.2.0.02,4]heptanes. Tetrahedron, 59: 2561-2565.
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  26. Dodziuk, H., A. Ejchart, W. Anczewski, H. Ueda, E. Krinichnaya, G. Dolgonos and W. Kutner, 2003. Water solubilization, determination of the number of different types of single-wall carbon nanotubes and their partial separation with respect to diameters by complexation with η-cyclodextrin. Chem. Commun., 2003: 986-987.
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  27. Anczewski, W., H. Dodziuk and A. Ejchart, 2003. Manifestation of chiral recognition of camphor enantiomers by alpha-cyclodextrin in longitudinal and transverse relaxation rates of the corresponding 1:2 complexes and determination of the orientation of the guest inside the host capsule. Chirality, 15: 654-659.
    PubMed  |  
  28. Jaszunski, M., G. Dolgonos and H. Dodziuk, 2002. An ab initio study of NMR chemical shifts and spin-spin coupling constants of bicyclobutane. Theor. Chem. Acc., 108: 240-245.
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  29. Dodziuk, H., 2002. Rigidity versus flexibility. A review of experimental and theoretical studies pertaining to the cyclodextrins nonrigidity. J. Mol. Struct., 614: 33-45.
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  30. Dodziuk, H., 2002. Among synthetic, supramolecular and theoretical chemistry: Stabilization of short-lived species in 'Molecular' or 'supramolecular flasks'. Int. J. Molec. Sci., 3: 814-821.
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  31. Dodziuk, H. and G. Dolgonos, 2002. Molecularmodelingstudy of hydrogen storage in carbonnanotubes. Chem. Phys. Lett., 356: 79-83.
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  32. Pecul, M., H. Dodziuk, M. Jaszunski, O. Lukin and J. Leszczynski, 2001. Ab initio calculations of the NMR spectra of [1.1.1]propellane and bicyclo[1.1.1]pentane. Phys. Chem. Chem. Phys., 3: 1986-1991.
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  33. Dodziuk, H., J. Leszczynski and K. Jackowski, 2001. Quantum chemical study of spiropentane, spiropentene and spiropentadiene. Tetrahedron, 57: 5509-5509.
  34. Dodziuk, H., G. Dolgonos and O. Lukin, 2001. Molecular mechanics study of endohedral fullerene complexes with small molecules. Carbon, 39: 1907-1911.
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  35. Dodziuk, H., 2001. Molecular and chiral recogition by cyclodextrins: A minireview. Biol. J. Armen., 53: 282-287 53: 282-287.
  36. Dodziuk, H., W. Kozminski, O. Lukin, D. Sybilska, 2000. NMR Manifestations and molecular modeling of chiral recognition of α-pinenes by α-Cyclodextrin. J. Mol. Structure, 523: 205-205.
  37. Dodziuk, H., O. Lukin and K.S. Nowinski, 2000. Molecularmechanics calculations of molecular and chiralrecognition by cyclodextrins. Is it reliable? The selectivecomplexation of decalins by β-cyclodextrin. J. Mol. Struct.: THEOCHEM, 503: 221-230.
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  38. Dodziuk, H., G. Dolgonos and O. Lukin, 2000. Ease of formation of nested fullerenes. Chem. Phys. Lett., 329: 351-356.
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  39. Dodziuk, H. and O. Lukin, 2000. The dependence of the average energy difference for the diastereomeric complexes of α-pinene enantiomers with α-cyclodextrin on the length of dynamic simulations. Chem. Phys. Lett., 327: 18-22.
  40. Dodziuk, H. and O. Lukin, 2000. Modeling of molecular and chiral recognition by cyclodextrins. Is it reliable? Part 2. Molecular dynamics calculations in vacuum pertaining to the selective complexation of decalins by β-cyclodextrin. Pol. J. Chem., 74: 997-1001.
  41. Dodziuk, H., J. Jurczak, W. Kozminski, O. Lukin, J. Sitkowski and L. Stefaniak, 2000. Dynamic NMR Study of Self-inclusion of a pendant group in amphiphilic 6-thiophenyl-6-deoxy-cyclodextrins. J. Mol. Structure, 519: 33-36.
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  42. Dodziuk, H., O. Lukin, K.S. Nowinski, 1999. Topological 'In'-'Out'Isomerism in perhydrogenated fullerenes revisited. C60H58R1R2 with two R groups Pol. J. Chem., 73: 299-306.
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  43. Dodziuk, H., K. Jackowski and J. Leszczynski, 1999. GIAO-CHF calculations of NMR chemical shifts for saturated hydrocarbons with unusual spatial structure. Proceedings of the International Conference on Progress in Computing of Physicochemical Properties, November 18-20, 1999, Warsaw, Poland -.
  44. Dodziuk, H., J. Leszczyński, K. Jackowski, 1999. Small-ring Geminanes-new hypothetical molecules with inverted carbon atoms. J. Org. Chem., 64: 6177-6181.
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  45. Dodziuk, H., A. Ejchart, O. Lukin and M.O. Vysotsky, 1999. 1H and 13C NMR and molecular dynamics study of chiral recognition of camphor enantiomers by α-cyclodextrin. J. Org. Chem., 64: 1503-1507.
    CrossRef  |  
  46. Dodziuk, H. and K.S. Nowiński, 1998. 'In'-'Out' topological isomerism. Should rotaxanes and endohedral fullerene complexes be involved?. Tetrahedron, 54: 2917-2930.
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  47. Dodziuk, H. and J. Leszczynski, 1998. Stretching the limits: According to High-level Ab Initio calculations C-o bonds are longer than the central C-C One in hypothetical 2-oxabicyclobutane. Pol. J. Chem., 72: 2030-2030.
  48. Dodziuk, H., J. Sitkowski, L. Stefaniak, D. Sybilska, J. Jurczak and K. Chmurski, 1997. Structure of cyclodextrins and their complexes. Part 6. The NMR observation of separate signals of host and guest pertaining to 1 : 1 and 1 : 2 complexes of 1,8-dimethylnaphthalene with β cyclodextrin. Pol. J. Chem., 71: 757-757.
  49. Dodziuk, H., J. Leszczynski and K.S. Nowinski, 1997. The quest for a planar and pyramidal carbon atom Part 4: An unsuccessful search for pyramidal carbon atoms in hypothetical unsaturated conjugated paddlane. J. Mol. Structure: THEOCHEM, 391: 201-205.
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  50. Dodziuk, H., J. Sitkowski, L. Stefaniak and D. Sybilska, 1996. Structure of cyclodextrins and their complexes. Part 7. Unusual NMR manifestations of chiral recognition of (1R, 5R)- and (1S, 5S)-α-pinenes by α-cyclodextrin in different solvents. Pol. J. Chem., 70: 1361-1361.
  51. Dodziuk, H., 1996. The classification scheme of isomers of organic molecules. Tetrahedron, 52: 12941-12946.
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  52. Dodziuk, H. and K. Nowinski, 1996. Horrorvacui' or topological in-outisomerism in perhydrogenatedfullerenes: C60H60 and monoalkylatedperhydrogenatedfullerenes. Chem. Phys. Lett., 249: 406-412.
    CrossRef  |  
  53. Dodziuk, H., J. Sitkowski, L. Stefaniak, D. Sybilska and J. Jurczak, 1995. Structure of cyclodextrins and their complexes. Part 51. The NMR observation of separate signals of host and guest pertaining to 1 : 1 and 1 : 2 complexes of acenaphthene with β cyclodextrin. Supramol. Chem., 7: 33-35.
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  54. Dodziuk, H., J. Leszczynski and K. Nowinski, 1995. In quest for planar and pyramidal carbon atom. Part 3. Can a tetrahedrally coordinated carbon form a nearly linear C C C bond angle?. J. Org. Chem., 60: 6860-6863.
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  55. Dodziuk, H., D. Sybilska, S. Miki, Z. Yoshida and J. Sitkowskia et al., 1994. Structure of cyclodextrins and their complexes. Part 4. Chromatographic and NMR Study of 1,2,3-tri-t-butylnaphthalene and its complex with γ-cyclodextrin. Tetrahedron, 50: 3619-3626.
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  56. Dodziuk, H., 1994. ChemInform abstract: Unusual saturated hydrocarbons: Interaction between theoretical and synthetic chemistry. ChemInform, Vol. 25 10.1002/chin.199442320.
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  57. Dodziuk, H. and K.S. Nowinski, 1994. In quest for planar and pyramidal carbon atom Part 2. AM1study of small bridged spiropentanes. J. Mol. Structure: THEOCHEM, 311: 97-100.
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  58. Dodziuk, H. and K. Nowinski, 1994. Structure of cyclodextrins and their complexes: Part 2. Do cyclodextrins have a rigid truncated-cone structure?. J. Mol. Structure: THEOCHEM, 304: 61-68.
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  59. Sybilska, D., M. Asztemborska, A. Bielejewska, J. Kowalczyk and H. Dodziuk et al., 1993. Chromatographic studies on the inclusion of isomeric dimethylnaphthalenes by β- and γ-cyclodextrin. Chromatographia, 35: 637-642.
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  60. Dodziuk, H., J. Sitkowski, L. Stefaniak, J. Jurczak and D. Sybilska, 1993. Structure of cyclodextrins and their complexes. Part 3. 1H NMR spectra of diastereomeric complexes of cis-decalin with β-cyclodextrin1. Supramol. Chem., 3: 79-81.
    CrossRef  |  
  61. Dodziuk, H., J. Sitkowski, L. Stefaniak, I.G. Mursakulov, I.G. Gasanov and V.A. Kurbanova, 1992. Conformational analysis of spiranes. Part III. Manifestation of chirality in the NMR spectra of spirobisdioxanes at low temperatures. Struct. Chem., 3: 269-276.
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  62. Dodziuk, H., 1992. Chirality and stereogenicity: The importance of conformational chirality in the classification of stereoisomers. Tetrahedron Asymm., 3: 43-43.
  63. Dodziuk, H., 1990. Bowlane (tetracyclo[3.3.3.13,10.17,10]tridecane) : A new hypothetical molecule possessing pyramidal tetracoordinated carbon atom in the ground state. (In quest for planar and pyramidal carbon atom. Part I). J. Mol. Struct., 239: 167-172.
  64. Dodziuk, H., 1990. A molecular mechanics study of C8H8 saturated cage compounds. Bull. Acad. Sci. Polon., Ser. Chim., 38: 11-11.
  65. Dodziuk, H. and M. Mirowicz, 1990. A proposal for a modification of the Cahn, Ingold and Prelog classification of chirality. Tetrahedron Asymm., 1: 171-186.
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  66. Chmielewski, M., Z. Kaluza, H. Dodziuk, K. Suwinska and D. Rosenbaum et al., 1990. Conformation of 2 C,1 N carbonyl-2 deoxy  D glyco-pyranosylamines. Carbohydr. Res., 203: 183-183.
  67. Dodziuk, H., 1988. A molecular mechanics study of new molecules containing inverted carbons: Small ring geminanes and [n.1.1]propellanes with n >4. Tetrahedron, 44: 2951-2955.
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  68. Dodziuk, H., 1987. The study of planarized and planar cyclohexane rings on the basis of molecular mechanics. Bull. Chem. Soc. Japan, 60: 3775-3775.
  69. Dodziuk, H. and K. Nowinski, 1987. Is hexaprismane the most stable isomer of C12H12 family of saturated cage compounds? Bull. Acad. Sci. Polon. Ser. Chim., 35: 195-195.
  70. Dodziuk, H., 1986. Conformational analysis of spiranes by the force field method. Part II. Heats of formation of small ring spiranes from spiro[2.2]pentane to spiro[5.5]undecane. Bull. Acad. Scie. Polon., Ser. Chim., 34: 49-49.
  71. Dodziuk, H., 1986. Conformation analysis of spiranes by the force-field method. Part 1. Chirality and diastereoisomerism of spiro-compounds: Spiro[5.5]undecane and derivatives. J. Chem. Soc., Perkin Trans. II, 1986: 249-251.
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  72. Dodziuk, H., 1984. Classical conformational analysis of strained organic molecules. I. [l,m,n]Propellanes with l,m,n equal to 2, 3, and 4. J. Comput. Chem., 5: 571-575.
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  73. Dodziuk, H., 1983. Molecular mechanics and rotational isomerism of di and trimethoxybenzenes. Pol. J. Chem., 57: 535-535.
  74. Dodziuk, H., H. Voithenberg, N.L. Allinger, 1982. A molecular mechanics study of methyl vinyl ether and related compounds. Tetrahedron, 38: 2811-2819.
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  75. Allinger, N.L., H. Dodziuk, D.W. Rogers and S.N. Naik, 1982. Heats of hydrogenation and formation of some 5 membered ring compounds by molecular mechanics calculations and direct measurements. Tetrahedron, 38: 1593-1593.
  76. Dodziuk, H., 1980. The role of electrostatic and nonbonded interactions in allylic and anomeric effects. Tetrahydropyran 2 ol. Pol. J. Chem., 54: 791-791.
  77. Dodziuk, H., 1979. The inapplicability of the MINDO/3 method to the conformational analysis of conjugated systems. J. Mol. Struct., 55: 107-111.
  78. Dodziuk, H., 1979. Nonbonded interactions and the allylic and anomeric effects. Carbohydr. Res., 70: 19-25.
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  79. Dodziuk, H., 1976. The influence of steric and electronic effects upon inversion barriers in simple aliphatic amines. Ann. Soc. Chim. Polon., 50: 1001-1001.
  80. Dodziuk, H., 1974. Steric effects in conjugated systems. VI. s cis s trans energy differences and barrier heights to internal rotation around Csp2 Csp2 bonds in monomethylated butadienes and acroleins. J. Mol. Struct., 20: 363-363.
  81. Dodziuk, H., 1974. Steric effects in conjugated systems. V. Methylvinyl ketone and methyl β N,N dimethylaminovinyl ketone. J. Mol. Struct., 20: 363-371.
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  82. Dodziuk, H., 1974. Nonbonded interactions and barrier heights for rotation of methyl group in monosubstituted propenes. Part II. 2 substituted propenes. Bull. Acad. Sci. Polon., Ser. Chim., 22: 75-75.
  83. Dodziuk, H., 1974. Nonbonded interactions and barrier heights for rotation of methyl group in monosubstituted propenes. Part I. s cis and s trans substituted propenes. J. Mol. Struct., 21: 29-29.
  84. Dodziuk, H., R.A. Kolinski and B. Korybut Daszkiewicz, 1973. Infrared spectra and structure of 1,4,8,11 tetraazacyclotetradecanes. Spectrochim. Acta, 29A: 511-511.
  85. Dodziuk, H., 1973. Steric effects in conjugated systems. IV. The barrier heights for the rotation of methyl group in monomethylated acroleins. Bull. Acad. Sci. Polon., Ser. Chim., 21: 627-627.
  86. Dodziuk, H., 1972. Steric effects in conjugated systems. III. The nonplanarity of 2,4 dimethylpentadiene 1,3. J. Mol. Struct., 14: 343-347.
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  87. Dodziuk, H., 1972. Steric effects in conjugated systems II. 2,3-Dimethylbutadiene. J. Mol. Struct., 12: 161-166.
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  88. Dodziuk, H., 1971. Steric effects in conjugated systems. I. Monosubstituted methylbutadienes. J. Mol. Struct., 10: 275-283.
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  89. Dodziuk, H., K. Kamienska Trela, J. Dabrowski, 1970. Infrared spectra and structure of unsaturated carbonyl compounds. Part III. Intensity measurements on enamino ketones of various configurations and conformations. Roczn. Chem., 44: 393-393.
  90. Miasek, M. and H. Dodziuk, 1967. Application of Houston's method to the sum of plane waves over the Brillouin zone. II. Body centered cubic lattice. J. Math. Phys., 48: 827-827.
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