Professor Andrzej Duda in memoriam

Penczek, S.; Lewinski, P.; Pretula, J.; Socka, M.

doi:10.14314/polimery.2017.239

Artykuł - szczegóły

Tytuł artykułu

Professor Andrzej Duda in memoriam

Autorzy

Penczek S. , Lewinski P. , Pretula J. , Socka M.

Treść / Zawartość

Pełne teksty:

Pobierz

Identyfikatory

DOI

10.14314/polimery.2017.239

Warianty tytułu

Pamięci Profesora Andrzeja Dudy

Języki publikacji

Abstrakty

This paper is describing major scientific achievements of the recently late Professor Andrzej Duda, Chairman of the Department of Polymer Chemistry of The Centre of Molecular and Macromolecular Studies of Polish Academy of Sciences. Professor Duda published over 100 scientific papers and has given several dozens of plenary and invited lectures at the scientific symposia. However, in the present paper, we are mostly describing accomplishment that all of us, and also Professor, have considered as his seminal work, that solved a long time controversial subject. Namely, how to influence reactivities of chiral monomers, using chiral catalysts. Professor Duda had shown, and this subject is mostly described, that reactivity of a chiral monomer can be unchanged (when compared with an achiral catalyst) when polymerized with catalyst of the same chirality and may be many times depressed (the feature highly valuable in several instances) when polymerized with a catalyst with an opposite chirality. This feature is very important in the copolymerization processes, when chiral monomer is much more reactive than the other comonomer. Besides, some other contributions of Professor Duda to Polymer Sciences are also, although briefly mentioned. Full list of papers is given in the second part of the paper.

Przedstawiono najważniejsze osiągnięcia naukowe Profesora Andrzeja Dudy, wieloletniego Kierownika Zakładu Chemii Polimerów Centrum Badań Molekularnych i Makromolekularnych Polskiej Akademii Nauk. Profesor Duda opublikował ponad 100 prac naukowych, wygłosił kilkadziesiąt wykładów na zaproszenie, w tym także wykłady plenarne na prestiżowych konferencjach międzynarodowych. W niniejszym, krótkim omówieniu prac Profesora skupiliśmy się przede wszystkim na dwóch zagadnieniach, spośród których szczególnie pierwsze było według naszego przekonania głównym osiągnięciem, rozwiązującym ważny problem dotyczący kopolimeryzacji monomerów chiralnych. Profesor Duda, po raz pierwszy w chemii polimerów, ustalił że polimeryzacja chiralnych monomerów przebiega niezmiennie wobec katalizatorów achiralnych oraz chiralnych o takim samym znaku jak znak monomeru, natomiast zastosowanie katalizatora o odwrotnej chiralności pozwala na znaczne zmniejszenie szybkości polimeryzacji. Jest to zjawisko o zasadniczym znaczeniu w kopolimeryzacji, szczególnie kiedy chiralny monomer jest znacznie bardziej reaktywny niż drugi komonomer. Mniej szczegółowo omówiono inne osiągnięcia Profesora Andrzeja Dudy, dodano też pełną bibliografię Jego prac.

Słowa kluczowe

chiral monomers comonomers reactivity polymerization rate of copolymerization

chiralne monomery komonomery reaktywność polimeryzacja szybkość kopolimeryzacji

Wydawca

Sieć Badawcza Łukasiewicz – Instytut Chemii Przemysłowej

Czasopismo

Polimery

Rocznik

2017

Tom

T. 62, nr 4

Strony

239--253

Opis fizyczny

Bibliogr. 24 poz., rys. kolor.

Twórcy

autor

Penczek S.

spenczek@cbmm.lodz.pl

Centre of Molecular and Macromolecular Studies of Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz, Poland

autor

Lewinski P.

Centre of Molecular and Macromolecular Studies of Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz, Poland

autor

Pretula J.

Centre of Molecular and Macromolecular Studies of Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz, Poland

autor

Socka M.

Centre of Molecular and Macromolecular Studies of Polish Academy of Sciences, Sienkiewicza 112, 90-363 Lodz, Poland

Bibliografia

[1] Majerska K., Duda A.: Journal of the American Chemical Society 2004, 126, 1026. http://dx.doi.org/10.1021/ja0388966
[2] Vion J.M., Jerome R., Teyssie P.: Macromolecules 1986, 19, 1828. http://dx.doi.org/10.1021/ma00161a009
[3] Kasperczyk J., Bero M.: Macromolecular Chemistry and Physics 1991, 192, 1777. http://dx.doi.org/10.1002/macp.1991.021920812
[4] Florczak M., Duda A.: Angewandte Chemie International Edition 2008, 47, 9088. http://dx.doi.org/10.1002/anie.200803540
[5] Van Beylen M., Morita H.: Macromolecular Symposia 2011, 308, 12. http://dx.doi.org/10.1002/masy.201151003
[6] Korotkov A.A.: Angewandte Chemie 1958, 70, 85. http://dx.doi.org/10.1002/ange.19580700313
[7] O’Driscoll K.F., Kuntz J.: Journal of Polymer Science Part A: Polymer Chemistry 1962, 61, 19. http://dx.doi.org/10.1002/pol.1962.1206117104
[8] Elias H.G.: “Macromolecules” vol. I, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 2005, p. 426.
[9] Eldessouki M., Gowayed Y., Acevedo O.: 6th International Conference on Nanomaterials NANOCON 2014, Brno, Czech Republik, November 5–7, 2014, p. 280.
[10] Aleman C., Bertran O., Houk K.N. et al.: Theoretical Chemistry Accounts 2012, 131, 1133. http://dx.doi.org/10.1007/s00214-012-1133-y
[11] Nomura N., Akita A., Ishii R. et al.: Journal of the American Chemical Society 2010, 132, 1750. http://dx.doi.org/10.1021/ja9089395
[12] Socka M., Duda A., Adamus A. et al.: Polymer 2016, 87, 50. http://dx.doi.org/10.1016/j.polymer.2016.01.059
[13] Duda A., Penczek S.: Macromolecular Rapid Communications 1994, 15, 559. http://dx.doi.org/10.1002/marc.1994.030150617
[14] Duda A., Penczek S.: Macromolecules 1994, 27, 4867. http://dx.doi.org/10.1021/ma00096a002
[15] Duda A., Penczek S.: Macromolecular Symposia 1991, 47, 127. http://dx.doi.org/10.1002/masy.19910470111
[16] Van Beylen M., Bywater S., Smets G. et al.: Advances in Polymer Science 1988, 86, 87. http://dx.doi.org/10.1007/BFb0025275
[17] Kunkel D., Muller A.H.E., Janata M., Lochman L.: Macromolecular Symposia 1992, 60, 315. http://dx.doi.org/10.1002/masy.19920600128
[18] Kazanskii K.S., Solovyanov A.A., Entelis S.G.: European Polymer Journal 1971, 7, 1421. http://dx.doi.org/10.1016/0014-3057(71)90036-X
[19] Wilczek L., Kennedy J.P.: Polymer Journal 1987, 19, 531. http://dx.doi.org/10.1295/polymj.19.531
[20] Kowalski A., Libiszowski J., Duda A., Penczek S.: Macromolecules 2000, 33, 1964. http://dx.doi.org/10.1021/ma991751s
[21] Kowalski A., Duda A., Penczek S.: Macromolecular Rapid Communications 1998, 19, 567. http://dx.doi.org/10.1002/(SICI)1521-3927(19981101)19:11<567::AID-MARC567>3.0.CO;2-T
[22] Kowalski A., Duda A., Penczek S.: Macromolecules 2000, 33, 689. http://dx.doi.org/10.1021/ma9906940
[23] Kowalski A., Duda A., Penczek S.: Macromolecules 2000, 33, 7359. http://dx.doi.org/10.1021/ma000125o
[24] Penczek S., Slazak R., Duda A.: Nature 1978, 273, 738. http://dx.doi.org/10.1038/273738a0
THE COMPLETE BIBLIOGRAPHY OF PROFESSOR ANDRZEJ DUDA
I. Research papers:
(1) Socka M., Duda A., Adamus A., Wach R.A., Ulanski P.: “Lactide/trimethylene carbonate triblock copolymers: Controlled sequential polymerization and properties”, Polymer 2016, 87, 50. http://dx.doi.org/10.1016/j.polymer.2016.01.059
(2) Basko M., Duda A., Kazmierski S., Kubisa P.: “Cationic copolymerization of racemic-beta-butyrolactone with L,L-lactide: One-pot synthesis of block copolymers”, Journal of Polymer Science Part A: Polymer Chemistry 2013, 51, 4873. http://dx.doi.org/10.1002/pola.26916
(3) Vachaudez M., D’hooge D.R., Socka M., Libiszowski J., Coulembier O., Reyniers M.F., Duda A., Marin G.B., Dubois Ph.: “Inverse dependencies on the polymerization rate in atom transfer radical polymerization of N-isopropylacrylamide in aqueous medium”, Reactive & Functional Polymers 2013, 73, 484. http://dx.doi.org/10.1016/j.reactfunctpolym.2012.11.004
(4) Miksa B., Sochacki M., Libiszowski J., Duda A., Ciesielski W., Potrzebowski M.J.: “Application of ionic liquid matrices in spectral analysis of poly(lactide) – solid state NMR spectroscopy versus matrix-assisted laser desorption/ionization time-of-flight (MALDI--TOF) mass spectrometry”, Analytical Methods 2012, 4, 377. http://dx.doi.org/10.1039/c2ay05332b
(5) Sroka-Bartnicka A., Ciesielski W., Libiszowski J., Duda A., Sochacki M., Potrzebowski M.J.: “Complementarity of solvent-free MALDI TOF and solid-state NMR spectroscopy in spectral analysis of polylactides”, Analytical Chemistry 2010, 82, 323. http://dx.doi.org/10.1021/ac9020006
(6) Danko M., Libiszowski J., Wolszczak M., Racko D., Duda A.: “Fluorescence study of the dynamics of a star-shaped poly(ε-caprolactone)s in THF: A comparison with a star-shaped poly(L-lactide)s”, Polymer 2009, 50, 2209. http://dx.doi.org/10.1016/j.polymer.2009.03.027
(7) Florczak M., Duda A.: “Effect of the configuration of the active center on comonomer reactivities: The case of ε-caprolactone/L,L-lactide copolymerization”, Angewandte Chemie International Edition 2008, 47, 9088. http://dx.doi.org/10.1002/anie.200803540
(8) Tomaszewski W., Duda A., Szadkowski M., Libiszowski J., Ciechanska D.: “Poly(L-lactide) nano- and microfibers by electrospinning: influence of poly(L-lactide) molecular weight”, Macromolecular Symposia 2008, 272, 70. http://dx.doi.org/10.1002/masy.200851209
(9) Florczak M., Libiszowski J., Mosnacek J., Duda A., Penczek S.: “L,L-lactide and ε-caprolactone block copolymers by a ‘poly(L,L-lactide) first’ route”, Macromolecular Rapid Communications 2007, 28, 1385. http://dx.doi.org/10.1002/marc.200700160
(10) Kowalski A., Libiszowski J., Majerska K., Duda A., Penczek S.: “Kinetics and mechanism of ε-caprolactone and L,L-lactide polymerization initiated with zinc octoate and aluminum tris-acetylacetonate: the next proofs for the general alkoxide mechanism and synthetic applications”, Polymer 2007, 48, 3952. http://dx.doi.org/10.1016/j.polymer.2007.05.007
(11) Florczak M., Kowalski A., Libiszowski J., Majerska K., Duda A.: “Application of the 27Al NMR spectroscopy to studies of polymerization mechanisms”, Polimery 2007, 52 (10), 722.
(12) Biela T., Duda A., Penczek S.: “Enhanced melt stability of star-shaped stereocomplexes as compared with linear stereocomplexes”, Macromolecules 2006, 39, 3710. http://dx.doi.org/10.1021/ma060264r
(13) Libiszowski J., Kowalski A., Biela T., Cypryk M., Duda A., Penczek S.: “Kinetics and mechanism of cyclic esters polymerization initiated with tin(II) octoate. Polymerization of ε-caprolactone and L,L--lactide coinitiated with primary amines”, Macromolecules 2005, 38, 8170. http://dx.doi.org/10.1021/ma050752j
(14) Duda A., Libiszowski J., Mosnáček J., Penczek S.: “Copolymerization of cyclic esters at the living polymer-monomer equilibrium”, Macromolecular Symposia 2005, 226, 109. http://dx.doi.org/10.1002/masy.200550811
(15) Danko M., Libiszowski J., Biela T., Wolszczak M., Duda A.: “Molecular dynamics of star-shaped poly(L-lactide)s in tetrahydrofuran as solvent monitored by fluorescence spectroscopy”, Journal of Polymer Science Part A: Polymer Chemistry 2005, 43, 4586. http://dx.doi.org/10.1002/pola.20932
(16) Biela T., Duda A., Pasch H., Rode K.: “Star-shaped poly(L-lactide)s with variable numbers of hydroxyl groups at polyester arms chain-ends and directly attached to the star-shaped core – controlled synthesis and characterization”, Journal of Polymer Science Part A: Polymer Chemistry 2005, 43, 6116. http://dx.doi.org/10.1002/pola.21035
(17) Duda A., Kowalski A., Libiszowski J., Penczek S.: “Thermodynamic and kinetic polymerizability of cyclic esters”, Macromolecular Symposia 2005, 224, 71. http://dx.doi.org/10.1002/masy.200550607
(18) Mosnáček J., Duda A., Libiszowski J., Penczek S.: “Copolymerization of L,L-lactide at its living polymer-monomer equilibrium with ε-caprolactone as comonomer”, Macromolecules 2005, 38, 2027. http://dx.doi.org/10.1021/ma0480446
(19) Libiszowski J., Kowalski A., Biela T., Duda A.: “Thermal stability of poly(L-lactide) prepared by polymerization of L,L-lactide with Sn(II) based initiators”, Polimery 2004, 49, 690.
(20) Duda A., Majerska K.: “Stereocontrolled polymerization of racemic lactide: combining stereoelection and chiral ligand-exchange mechanism”, Journal of The American Chemical Society 2004, 126, 1026. http://dx.doi.org/10.1021/ja0388966
(21) Libiszowski J., Kowalski A., Szymanski R., Duda A., Raquez J.-M., Degee P., Dubois P.: “Monomer–linear macromolecules–cyclic oligomers equilibria in the polymerization of 1,4-dioxan-2-one”, Macromolecules 2004, 37, 52. http://dx.doi.org/10.1021/ma030244e
(22) Penczek S., Szymanski R., Duda A., Baran J.: “Living polymerization of cyclic esters – a route to (bio)degradable polymers. Influence of chain transfer to polymer on livingness”, Macromolecular Symposia 2003, 201, 261. http://dx.doi.org/10.1002/masy.200351129
(23) Biela T., Duda A., Rode K., Pasch H.: “Characterization of star-shaped poly(L-lactide)s in two-dimensional chromatography”, Polymer 2003, 44, 1851. http://dx.doi.org/10.1016/S0032-3861(03)00030-2
(24) Ydens I., Degee P., Dubois P., Libiszowski J., Duda A., Penczek S.: “Combining ATRP of methacrylates and ROP of L,L-dilactide and ε-caprolactone”, Macromolecular Chemistry and Physics 2003, 204, 171. http://dx.doi.org/10.1002/macp.200290071
(25) (a) Ydens I., Degee P., Libiszowski J., Duda A., Penczek S., Dubois P.: “Controlled synthesis of amphiphilic poly(methyl methacrylate)-g-[poly(ester)/poly(ether)] graft terpolymers”, American Chemical Society Division of Polymer Chemistry. Polymer Preprints 2002, 42 (2), 39; (b) Ydens I., Degee P., Libiszowski J., Duda A., Penczek S., Dubois P.: “Controlled synthesis of am250phiphilic poly(methyl methacrylate)-g-[poly(ester)/poly(ether)] graft terpolymers” in “Advances in controlled/living radical polymerization” (Ed. Matyjaszewski K.), (American Chemical Sciety, Symposium Series 854), American Chemical Society, Washington DC 2003, pp. 283–298.
(26) Biela T., Duda A., Penczek S.: “Control of Mn, Mw/Mn, end-groups, and kinetics in living polymerization of cyclic esters”, Macromolecular Symposia 2002, 183, 1. http://dx.doi.org/10.1002/1521-3900(200207)183:1<1::AID-MASY1>3.0.CO;2-Q
(27) Biela T., Duda A., Penczek S., Rode K., Pasch H.: “Well-defined star polylactides and their behaviour in two-dimensional chromatography”, Journal of Polymer Science, Part A: Polymer Chemistry 2002, 40, 2884. http://dx.doi.org/10.1002/pola.10366
(28) Kulshrestha S., Libiszowski J., Duda A., Penczek S., Gross R.: “Enzyme catalyzed lactone polymerizations: end group functionalization”, American Chemical Society Division of Polymer Chemistry. Polymer Preprints 2002, 42 (2), 1205.
(29) Duda A., Kowalski A., Penczek S., Uyama H., Kobayashi S.: “Kinetics of the ring-opening polymerization of 6-, 7-, 9-, 12-, 13-, 16-, and 17-membered lactones. Comparison of chemical and enzymatic polymerization”, Macromolecules 2002, 35, 4266. http://dx.doi.org/10.1021/ma012207y
(30) Libiszowski J., Kowalski A., Duda A., Penczek S.: “Kinetics and mechanism of cyclic esters polymerization initiated with covalent metal carboxylates. 5. End-group studies in the model ε-caprolactone and L,L-dilactide/tin(II) and zinc octoate/butyl alcohol systems”, Macromolecular Chemistry and Physics 2002, 203, 1694. http://dx.doi.org/10.1002/1521-3935(200207)203:10/11<1694::AID-MACP1694>3.0.CO;2-J
(31) Majerska K., Duda A., Penczek S.: “Kinetics and mechanism of cyclic esters polymerization initiated with tin(II) octoate. 4. Influence of 2,6-ditertbutylpyridine on kinetics of polymerization of ε-caprolactone and L,L-dilactide”, Macromolecular Rapid Communications 2000, 21, 1327. http://dx.doi.org/10.1002/1521-3927(20001201)21:18<1327::AID-MARC1327>3.3.CO;2-0
(32) Kowalski A., Duda A., Penczek S.: “Kinetics and mechanism of cyclic esters polymerization initiated with tin(II) octoate. 3. Polymerization of L,L-dilactide”, Macromolecules 2000, 33, 7359. http://dx.doi.org/10.1021/ma000125o
(33) Penczek S., Duda A., Kowalski A., Libiszowski J., Majerska K., Biela T.: “On the mechanism of polymerization of cyclic esters induced by tin(II) octoate”, Macromolecular Symposia 2000, 157, 61. http://dx.doi.org/10.1002/1521-3900(200007)157:1<61::AID-MASY61>3.0.CO;2-6
(34) Penczek S., Biela T., Duda A.: “Living polymerization with reversible chain transfer and reversible deactivation: the case of cyclic esters”, Macromolecular Rapid Communications 2000, 21, 941. http://dx.doi.org/10.1002/1521-3927(20000901)21:14<941::AID-MARC941>3.0.CO;2-R
(35) Duda A., Penczek S., Kowalski A., Libiszowski J.: “Polymerizations of ε-caprolactone and L,L-dilactide initiated with stannous octoate and stannous butoxide - a comparison”, Macromolecular Symposia 2000, 153, 41. http://dx.doi.org/10.1002/1521-3900(200003)153:1<41::AID-MASY41>3.0.CO;2-I
(36) Kowalski A., Libiszowski J., Duda A., Penczek S.: “Polymerization of L,L-dilactide initiated by tin(II) butoxide”, Macromolecules 2000, 33, 1964. http://dx.doi.org/10.1002/1521-3900(200003)153:1<41::AID-MASY41>3.0.CO;2-I
(37) Kowalski A., Duda A., Penczek S.: “Kinetics and mechanism of cyclic esters polymerization initiated with tin(II) octoate. 2. Macromolecules fitted with tin(II) alkoxide species observed directly in MALDI--TOF spectra”, Macromolecules 2000, 33, 689. http://dx.doi.org/10.1021/ma9906940
(38) Penczek S., Duda A., Kowalski A., Libiszowski J.: “Controlled polymerization of cyclic esters. Covalent metal alkoxides vs carboxylates: Sn(OC4H9)2 vs Sn(OC(O)C7H15)2 (viz. Sn(Oct)2)”, Polymeric Materials – Science and Engineering 1999, 80, 95.
(39) Kowalski A., Libiszowski J., Duda A., Penczek S.: “Kinetics and mechanism of polymerization of cyclic esters”, American Chemical Society Division of Polymer Chemistry. Polymer Preprints 1998, 39 (2), 74.
(40) Kowalski A., Duda A., Penczek S.: “Kinetics and mechanism of cyclic esters polymerization initiated with tin(II) octoate. 1. Polymerization of ε-caprolactone”, Macromolecular Rapid Communications 1998, 19, 567. http://dx.doi.org/10.1002/(SICI)1521-3927(19981101)19:11<567::AID-MARC567>3.0.CO;2-T
(41) Penczek S., Duda A., Libiszowski J.: “Controlled polymerization of cyclic esters. Structure of initiators and of active species related to the selectivity of initiation and propagation”, Macromolecular Symposia 1998, 128, 241. http://dx.doi.org/10.1002/masy.19981280123
(42) Penczek S., Duda A., Szymanski R.: “Intra- and intermolecular chain transfer to macromolecules with chain scission. The case of cyclic esters”, Macromolecular Symposia 1998, 132, 441. http://dx.doi.org/10.1002/masy.19981320141
(43) Kowalski A., Duda A., Penczek S.: “Polymerization of L,L-lactide initiated with aluminum isopropoxide trimer or tetramer”, Macromolecules 1998, 31, 2114. http://dx.doi.org/10.1021/ma971737k
(44) Duda A., Biela T., Libiszowski J., Penczek S., Dubois P., Mecerreyes D., Jerome R.: “Block and random copolymers of ε-caprolactone”, Polymer Degradation and Stability 1998, 59, 215. http://dx.doi.org/10.1016/S0141-3910(97)00167-5
(45) Simic V., Girardon V., Spassky N., Hubert-Pfalzgraf L.G., Duda A.: “Ring-opening polymerization of lactides initiated with yttrium tris-isopropoxyethoxide”, Polymer Degradation and Stability 1998, 59, 227. http://dx.doi.org/10.1016/S0141-3910(97)00200-0
(46) Duda A.: “Broadening of the polymerization degree distribution in living polymerization”, Polimery 1998, 43, 135.
(47) Baran J., Duda A., Kowalski A., Szymanski R., Penczek S.: “Intermolecular chain transfer to polymer with chain scission: General treatment and determination of kp/ktr in L,L-lactide polymerization”, Macromolecular Rapid Communications 1997, 18, 325. http://dx.doi.org/10.1002/marc.1997.030180409
(48) Baran J., Duda A., Kowalski A., Szymanski R., Penczek S.: “Quantitative comparison of selectivities in the polymerization of cyclic esters”, Macromolecular Symposia 1997, 123, 93. http://dx.doi.org/10.1002/masy.19971230110
(49) Duda A.: “Polymerization of ε-caprolactone initiated by aluminum isopropoxide carried out in the presence of alcohols and diols. Kinetics and mechanism”, Macromolecules 1996, 29, 1399. http://dx.doi.org/10.1021/ma951442b
(50) Duda A., Penczek S., Dubois P., Mecerreyes D., Jerome R.: “Oligomerization and copolymerization of γ-butyrolactone – a monomer known as unable to homopolymerize. 1. Copolymerization with ε-caprolactone”, Macromolecular Chemistry and Physics 1996, 197, 1273. http://dx.doi.org/10.1002/macp.1996.021970408
(51) Biela T., Duda A.: “Solvent effect in the polymerization of ε-caprolactone initiated with diethylaluminum ethoxide”, Journal of Polymer Science, Part A: Polymer Chemistry 1996, 34, 1807. http://dx.doi.org/10.1002/(SICI)1099-0518(19960715)34:9<1807::AID-POLA19>3.0.CO;2-A
(52) (a) Penczek S., Duda A., Szymanski R.: “Selectivity as a measure of »livingness«. The case of cyclic esters polymerization”, American Chemical Society Division of Polymer Chemistry. Polymer Preprints 1996, 37 (1), 219; (b) Penczek S., Duda A.: “Selectivity as a measure of »livingness« of the polymerization of cyclic esters”, Macromolecular Symposia 1996, 107, 1. http://dx.doi.org/10.1002/masy.19961070103
(53) Penczek S., Szymanski R., Duda A.: “Polymerization with contribution of covalent and ionic species”, Macromolecular Symposia 1995, 98, 193. http://dx.doi.org/10.1002/masy.19950980116
(54) Penczek S., Duda A.: “The kinetics and mechanism of ε-caprolactone polymerization initiated with covalent metal alkoxides”, Polymer Materials Science and Engineering 1995, 72, 228.
(55) Duda A., Penczek S.: “Polymerization of ε-caprolactone initiated by aluminum isopropoxide trimer and/or tetramer”, Macromolecules 1995, 28, 5981. http://dx.doi.org/10.1021/ma00122a001
(56) Duda A., Penczek S.: “On the difference of reactivities of various aggregated forms of aluminum isopropoxide in initiating ring-opening polymerizations”, Macromolecular Rapid Communications 1995, 16, 67. http://dx.doi.org/10.1002/marc.1995.030160112
(57) Biela T., Duda A., Penczek S.: “Factors affecting »livingness« in polymerization initiated with aluminum alkoxides”, American Chemical Society Division of Polymer Chemistry. Polymer Preprints 1994, 35 (2), 508.
(58) Duda A., Penczek S.: “Determination of the absolute propagation rate constants in polymerization with reversible aggregation of active centers”, Macromolecules 1994, 27, 4867. http://dx.doi.org/10.1021/ma00096a002
(59) Duda A.: “Preparation of telechelic polyester oligodiols by the chain-transfer polymerization of ε-caprolactone”, Macromolecules 1994, 27, 576. http://dx.doi.org/10.1021/ma00080a036
(60) Duda A., Penczek S.: “Kinetics of polymerization involving reversible deactivation due to aggregation of active centers. Analytical vs. numerical solution for the ε-caprolactone/dialkylaluminium alkoxide system”, Macromolecular Rapid Communications 1994, 15, 559. http://dx.doi.org/10.1002/marc.1994.030150617
(61) Penczek S., Duda A., Kaluzynski K., Lapienis G., Nyk A., Szymanski R.: “Thermodynamics and kinetics of ring-opening polymerization of cyclic alkylene phosphates”, Makromolekulare Chemie. Macromolecular Symposia 1993, 73, 91. http://dx.doi.org/10.1002/masy.19930730110
(62) Duda A.: “Anionic polymerization of 4-methyl-2-oxetanone (β-butyrolactone)”, Journal of Polymer Science, Part A: Polymer Chemistry 1992, 30, 21. http://dx.doi.org/10.1002/pola.1992.080300103
(63) (a) Penczek S., Duda A., Slomkowski S.: “Living pseudoanionic polymerization of lactones”, American Chemical Society Division of Polymer Chemistry. Polymer Preprints 1991, 32 (1), 306; (b) Penczek S., Duda A., Slomkowski S.: “The reactivity-selectivity principle. The case of polymerization of ε-CL”, Makromolekulare Chemie. Macromolecular Symposia 1992, 54/55, 31. http://dx.doi.org/10.1002/masy.19920540106
(64) Duda A., Penczek S.: “Kinetics of ε-caprolactone polymerization on dialkylaluminum alkoxides”, Makromolekulare Chemie. Macromolecular Symposia 1991, 47, 127. http://dx.doi.org/10.1002/masy.19910470111
(65) Penczek S., Duda A.: “Polymerization and copolymerization of elemental sulfur”, Phosphorus, Sulfur, and Silicon and the Related Elements, 1991, 59, 47. http://dx.doi.org/10.1080/10426509108045700
(66) (a) Duda A., Penczek S.: “Anionic and pseudoanionic polymerization of ε-caprolactone”, American Chemical Society Division of Polymer Chemistry. Polymer Preprints 1990, 30 (1), 12; (b) Duda A., Penczek S.: “Anionic and pseudoanonic polymerization of ε-caprolactone”, Makromolekulare Chemie. Macromolecular Symposia 1991, 42/43, 135. http://dx.doi.org/10.1002/masy.19910420110
(67) Duda A., Florjanczyk Z., Hofman A., Slomkowski S., Penczek S.: “Living pseudoanionic polymerization of ε-caprolactone. Poly(ε-caprolactone) free of cyclics and with controlled end-groups”, Macromolecules 1990, 23, 1640. http://dx.doi.org/10.1021/ma00208a013
(68) Duda A., Penczek S.: “Thermodynamics of L-lactide polymerization”, Macromolecules 1990, 23, 1636. http://dx.doi.org/10.1021/ma00208a012
(69) Labuk P., Duda A., Penczek S.: “Reaction of elemental sulfur with acrylonitrile”, Phosphorus, Sulfur, and Silicon and the Related Elements 1989, 42, 107. http://dx.doi.org/10.1080/10426508908054883
(70) Duda A., Penczek S.: “Liquid oligomeric diols with high sulfur content from elemental sulfur, cyclic sulfides and dihydroxypolysulfides”, Die Makromolekulare Chemie, Rapid Communications 1988, 9, 151. http://dx.doi.org/10.1002/marc.1988.030090307
(71) Sosnowski S., Duda A., Slomkowski S., Penczek S.: “Determination by 31P-NMR of the structure of active centers in the anionic polymerization. End-capping with a P-containing reagent”, Die Makromolekulare Chemie, Rapid Communications 1984, 5, 551. http://dx.doi.org/10.1002/marc.1984.030050912
(72) Baran T., Duda A., Penczek S.: “Anionic polymerization of exo-3,4,5-trithiatetracyclo[5.5.1.O2,6.O8,12]tridec--10-ene (dicyclopentadiene trisulfide)”, Die Makromolekulare Chemie 1984, 185, 2337. http://dx.doi.org/10.1002/macp.1984.021851111
(73) Baran T., Duda A., Penczek S.: “Anionic polymerization of norbornene trisulfide”, Journal of Polymer Science, Polymer Chemistry Edition 1984, 22, 1085. http://dx.doi.org/10.1002/pol.1984.170220509
(74) Duda A., Szymanski R., Penczek S.: “Anionic copolymerization of elemental sulfur with propylene sulfide. Equilibrium sulphur concentration”, Journal of Macromolecular Science: Part A–Chemistry 1983, 20, 967. http://dx.doi.org/10.1080/00222338308060805
(75) Sokolowska A., Duda A.: „Zastosowanie spektroskopii Ramana do badania kopolimeryzacji siarki elementarnej”, Polimery 1982, 27, 201.
(76) Duda A., Penczek S.: “Anionic copolymerization of elemental sulfur with propylene sulfide”, Macromolecules 1982, 15, 36. http://dx.doi.org/10.1021/ma00229a007
(77) Penczek S., Duda A.: “Anionic copolymerization of elemental sulfur”, Pure and Applied Chemistry 1981, 53, 1679. http://dx.doi.org/10.1351/pac198153091679
(78) Duda A., Penczek S.: “Anionic copolymerization of elemental sulfur with 2,2-dimethylthiirane”, Makromolecular Chemie 1980, 181, 995. http://dx.doi.org/10.1002/macp.1980.021810503
(79) Penczek S., Slazak R., Duda A.: “Anionic copolymerization of elemental sulphur”: (a) Nature 1978, 273, 738. http://dx.doi.org/10.1038/273738a0(b) Nature 1979, 280, 846. http://dx.doi.org/10.1038/280846c0
(80) Sugier H., Duda A.: “The γ-radiolysis of polycrystalline zinc oxide”, Radiochemical and Radioanalytical Letters 1977, 27, 359.
II. Reviews:
(1) Duda A., Kubisa P., Lapienis G., Slomkowski S.: “Milestones in development of a ring-opening polymerization of the heterocyclic monomers – view from a personal perspective”, Polimery 2014, 59, 9.
(2) Duda A., Kubisa P., Matyjaszewski K., Slomkowski S.: “Professor Stanislaw Penczek – the polymers world and not only”, Polimery 2014, 59, 3.
(3) Slomkowski S., Penczek S., Duda A.: “Polylactides - an overview”, Polymer Advanced Technology 2014, 25, 436.
(4) Raquez J.-M., Coulembier O., Duda A., Narayan R., Dubois P.: “Recent advances in the synthesis and applications of poly(1,4-dioxan-2-one)-based copolymers”, Polimery 2009, 54, 163.
(5) Penczek S., Cypryk M., Duda A., Kubisa P., Slomkowski S.: “Living ring-opening polymerizations of heterocyclic monomers”, Progress in Polymer Science 2007, 32, 247.
(6) Duda A., Kowalski A.: „Zdolność do polimeryzacji cyklicznych estrów alifatycznych”, Polimery 2007, 52, 487.
(7) Biela T., Kowalski A., Libiszowski J., Duda A., Penczek S.: “Progress in polymerization of cyclic esters: mechanism and synthetic applications”, Macromolecular Symposia 2006, 240, 47.
(8) Duda A., Biela T., Libiszowski J., Kowalski A.: “Amines as (co)initiators of cyclic esters polymerization”, Polimery 2005, 50, 501.
(9) Duda A.: “Stereocontrolled polymerization of chiral heterocyclic monomers”, Polimery 2004, 49, 469.
(10) Duda A., Penczek S.: „Polilaktyd [poli(kwas mlekowy)]: Synteza, właściwości i zastosowania”, Polimery 2003, 48, 16.
(11) Duda A.: “Controlled synthesis of poly(ε--caprolactone) and poly(L-lactide) of various architectures”, Polimery 2002, 47, 469.
(12) Penczek S., Duda A., Szymanski R., Biela T.: “What we have learned in general from cyclic esters polymerization”, Macromolecular Symposia 2000, 153, 1.
(13) Duda A., Kowalski A., Libiszowski J.: „Kinetyka i mechanizm polimeryzacji ε-kaprolaktonu inicjowanej oktanianem cynawym”, Polimery 2000, 45, 465.
(14) Duda A., Kubisa P., Penczek S.: “Progress in mechanistic studies of anionic and cationic polymerizations”, Indian Journal of Technology 1993, 31, 222.
(15) Duda A.: „Zastosowanie zasady łączącej reaktywność z selektywnością do analizy procesów polimeryzacji”, Polimery 1992, 37, 293.
(16) Duda A., Penczek S.: „Polimeryzacja jonowa i pseudojonowa”, Polimery 1989, 34, 429.
III. Chapters in encyclopedias and monographies:
(1) Duda A.: “ROP of cyclic esters. Mechanisms of ionic and coordination processes” in “Polymer Science: A Comprehensive Reference”, vol. 4, (Ed. Matyjaszewski K., Möller M.), Amsterdam: Elsevier BV 2012, pp. 213–245.
(2) Penczek S., Cypryk M., Duda A., Kubisa P., Slomkowski S.: “Living ring-opening polymerization of heterocyclic monomers” in “Controlled and living polymerizations. From mechanisms to applications”, Chapter 5, (Ed. Matyjaszewski K., Mueller A.H.E.), Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 2009, pp. 241–296.
(3) Duda A., Kowalski A.: “Thermodynamics and kinetics of ring-opening polymerization” in “Handbook of ring-opening polymerization”, Chapter 1, (Ed. Dubois Ph., Degee Ph., Coulembier O., Raquez J.-M.), Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 2009, pp. 1–51.
(4) Penczek S., Duda A., Kubisa P., Slomkowski S.: “Ionic and coordination ring-opening polymerization” in “Macromolecular engineering, precise synthesis, material properties, applications”, Vol. 1, Chapter 4 (Ed. Matyjaszewski K., Gnanou Y., Leilbler L.), Wiley--VCH Verlag GmbH & Co. KGaA, Weinheim 2007, pp. 103–159.
(5) Penczek S., Duda A., Kubisa P.: “Living ring-opening polymerizations of heterocyclic monomers” in “Living and controlled polymerization” (Ed. Grodzinski J.), Nova Science Publishers Inc., New York 2005, pp. 173–212.
(6) Duda A., Penczek S.: “Mechanisms of aliphatic polyester formation” in “Biopolymers”, Vol. 3b: “Polyesters II – Properties and chemical synthesis” (Ed. Steinbüchel A., Doi Y.), Wiley-VCH, Weinheim 2002, Chapter 12, pp. 371–430.
(7) Duda A., Penczek S.: “Thermodynamics, kinetics, and mechanism of cyclic esters polymerization” in “Polymers from renewable resources: biopolyesters and biocatalysis” (American Chemical Society, Symposium Series 764) (Ed. Scholz C., Gross R.A.), Oxford University Press – USA, Washington DC 2000, pp. 160–199.
(8) Penczek S., Duda A., Szymanski R., Baran J., Libiszowski J., Kowalski A.: “Kinetics of elementary reactions in cyclic esters polymerization” in “Ionic polymerizations and related processes”, (Ed. Puskas J.E. et al.), Kluwer Academic Publishers, Amsterdam 1999, pp. 283–299.
(9) Slomkowski S., Duda A.: “Anionic ring-opening polymerization” in “Ring-opening polymerization: mechanism, catalysis, structure, utility” (Ed. Brunelle D.J.), Hanser Publisher, New York 1993, pp. 87–128.
(10) (a) Duda A., Penczek S.: “Sulfur-containing polymers” in “Encyclopedia of polymer science and engineering” (Ed. Mark H. et al.), J. Wiley and Sons, New York 1989, vol. 16, pp. 246–368; (b) Duda A., Penczek S.: “ Sulfur-containing polymers” in “Concise encyclopedia of polymer science and engineering” (Ed. Mark H. et al.), J. Wiley and Sons, New York 1990, pp. 1141–1148.

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Opracowanie ze środków MNiSW w ramach umowy 812/P-DUN/2016 na działalność upowszechniającą naukę (zadania 2017).

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