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1
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C. M. Thiele, S. Berger, Probing the Diastereotopicity of Methylene Protons in Strychnine Using Residual Dipolar Couplings, Org. Lett. 2003, 5, 705-708.
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2
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C. M. Thiele, T. N. Mitchell, Hydrostannylation of Propargylic Alcohols Using Mixed Tin Hydrides, Eur. J. Org. Chem. 2004, 337-353.
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3
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C. M. Thiele, T. N. Mitchell, Stille Coupling Reactions of functionalised triorganotin halides, Appl. Organomet. Chem. 2004, 83-85.
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4
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C. M. Thiele, Poly-γ-ethyl-Lglutamate as Alignment Medium for the Measurement of RDCs in Organic Substrates, J. Org. Chem. 2004, 69, 7403-7413.
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5
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C. M. Thiele, Book Review, Structure Elucidation by NMR in Organic Chemistry, A practical guide. 3rd revised edn. by E. Breitmaier, Magn. Res. Chem. 2004, 42, 368.
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6
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C. M. Thiele, Scaling the alignment of Polyglutamates by Variable Angle Sample Spinning, Angew. Chem. 2005, 117, 2847-2850, Angew. Chem. Int. Ed. 2005, 44, 2787-2790.
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7
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V. V. Klochkov, A. V. Klochkov, C. M. Thiele, S. Berger, A Novel Liquid Crystalline System for Partial Alignment of Organic Molecules, J. Magn. Res. 2006, 179, 58-63.
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8
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C. M. Thiele, Book Review, Essential NMR, B. Blümich, Macromol. Chem. Phys. 2006, 207, 910.
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9
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C. M. Thiele, A. Marx, R. Berger, J. Fischer, M. Biel, A. Giannis, Determination of the relative configuration of a five-membered ring compound using RDCs, Angew. Chem. 2006, 118, 4566-4571, Angew. Chem. Int. Ed. 2006, 45, 4455-4460.
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10
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C. M. Thiele, Use of RDCs in Rigid Organic Compounds and Some Practical Considerations concerning Alignment Media, Conc. Magn. Res. 2007, 30A, 65-80 (Review).
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11
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C. M. Thiele, Magnetic Resonance at or below the Earth's magnetic field, Angew. Chem. 2007, 119, 4904-4909; Angew. Chem. Int. Ed. 2007, 46, 4820-24.
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12
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C. M. Thiele, W. Bermel, J-modulated ADEQUATE experiments using different kinds of refocusing pulses, Magn. Res. Chem. 2007, 45, 889-894.
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13
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S. Leuthäußer, V. Schmidts, C. M. Thiele, H. Plenio, π-Face Donor Properties of N-Heterocyclic Carbenes in Grubbs II Complexes, Chem. Eur. J. 2008, 14, 5465-5481.
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14
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C. M. Thiele, Residual Dipolar Couplings (RDCs) in Organic Structure Determination, Eur. J. Org. Chem. 2008, 5673-5685.
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15
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A. Marx, C. M. Thiele, Orientational properties of PBLG: Influence of molecular weight and solvent on order parameters of the solute, Chem. Eur. J. 2009, 15, 254-260.
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16
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R. S. Stoll, M. V. Peters, A. Kühn, S. Heiles, R. Goddard, M. Bühl, C. M. Thiele, S. Hecht, Photoswitchable Catalysts: Correlating Structure and Conformational Dynamics with Reactivity by a Combined Experimental and Computational Approach, J. Am. Chem. Soc. 2009, 131, 357-367.
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17
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C. M. Thiele, K. Petzold, J. Schleucher, EASY ROESY: Reliable Cross-Peak Integration in Adiabatic Symmetrized ROESY, Chem. Eur. J. 2009, 15, 585-588.
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18
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A. Marx, V. Schmidts, C. M. Thiele, How different are diastereomorphous orientations of enantiomers in the liquid crystalline phases of PBLG and PBDG: a case study, Magn. Res. Chem. 2009, 47, 734-740.
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19
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C. M. Thiele, V. Schmidts, B. Böttcher, I. Louzao, R. Berger, A. Maliniak, B. Stevensson, On the Treatment of Conformational Flexibility when using Residual Dipolar Couplings for Structure Determination, Angew. Chem. 2009, 121, 6836-6840, Angew. Chem. Int. Ed. 2009, 48, 6708-6712.
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20
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C. M. Thiele, A. Maliniak, B. Stevensson, Use of Local Alignment Tensors for the Determination of Relative Configurations in Organic Compounds, J. Am. Chem. Soc. 2009, 131, 12878-12879.
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21
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B. Böttcher, V. Schmidts, J. A. Raskatov, C. M. Thiele, Determination of the Conformation of the Key Intermediate in an Enantioselective Palladium-Catalyzed Allylic Substitution from Residual Dipolar Couplings, Angew. Chem. 2010, 122, 210-214, Angew. Chem. Int. Ed. 2010, 49, 205-209.
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22
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A. Marx, B. Böttcher, C. M. Thiele, Enhancing the Orienting Properties of Poly(γ-benzyl-L-glutamate) by means of Additives, Chem. Eur. J. 2010, 16, 1656-1663.
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23
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L. Arnold, A. Marx, C. M. Thiele, M. Reggelin, Polyguanidines as Chiral Orienting Media for Organic Compounds, Chem. Eur. J. 2010, 16, 10342-10346.
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24
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U. M. Reinscheid, M. Köck, C. Cychon, V. Schmidts, C. M. Thiele, C. Griesinger, The Absolute Configuration of Dibromopalau'amine, Eur. J. Org. Chem. 2010, 6900-6903.
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25
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C. M. Thiele, W. C. Pomerantz, N. L. Abott, S. H. Gellman, Lyotropic liquid crystalline phases from helical β-peptides as alignment media, Chem. Commun. 2011, 47, 502-504 (Emerging Investigators Issue).
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26
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D. Zornik, R. M. Meudtner, T. El Malah, C. M. Thiele, S. Hecht, Designing Structural Motifs for Clickamers: Exploiting the 1,2,3-Triazole Moiety to Generate Conformationally Restricted Architectures, Chem. Eur. J. 2011, 17, 1473-1484.
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27
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G. Kummerlöwe, S. L. Grage, C. M. Thiele, I. Kuprov, A. S. Ulrich, B. Luy, Variable Angle NMR Spectroscopy and Its Application to the Measurement of Residual Chemical Shift Anisotropy, J. Magn. Reson. 2011, 209, 19-30.
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28
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C. M. Thiele, W. Bermel, Speeding up the measurement of one-bond scalar (1J) and residual dipolar couplings (1D) by using non-uniform sampling (NUS), J. Magn. Reson. 2012, 216, 134-143 / Corrigendum.
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29
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B. Böttcher, C. M. Thiele, Determining the Stereochemistry of Molecules from Residual Dipolar Couplings (RDCs), in Encyclopedia of Magnetic Resonance, (published by R. K. Harris, R. E. Wasylishen), John Wiley, Chichester, 2012.
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30
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R. Berger, J. Courtieu, R. R. Gil, C. Griesinger, M. Köck, P. Lesot, B. Luy, D. Merlet, A. Navarro-Vázquez, M. Reggelin, U. M. Reinscheid, C. M. Thiele, M. Zweckstetter, Is Enantiomer Assignment Possible by NMR Spectroscopy Using Residual Dipolar Couplings from Chiral Nonracemic Alignment Media? – A Critical Assessment, Angew. Chem. 2012, 124, 8512–8515, Angew. Chem. Int. Ed. 2012, 51, 8388–8391.
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31
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N.-C. Meyer, A. Krupp, V. Schmidts, C. M. Thiele, M. Reggelin, Polyacetylenes as Enantiodifferentiating Alignment Media, Angew. Chem. 2012, 124, 8459–8463, Angew. Chem. Int. Ed. 2012, 51, 8334–8338.
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32
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H.-G. Weinig, C. M. Thiele, 4. Chinesisch-Deutsches Symposium “Frontiers of Chemistry”, Nachr. Chem. 2012, 60, 1234-1235.
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33
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P. Giraudeau, T. Montag, B. Charrier, C. M. Thiele, Fast access to residual dipolar couplings by single-scan 2D NMR in oriented media, Magn. Reson. Chem. 2012, 50, S53–S57 / Corrigendum.
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34
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T. Montag, C. M. Thiele, Cross-Linked Helically Chiral Poly-(γ-benzyl-L-glutamate) as Enantiodiscriminating Alignment Medium, Chem. Eur. J. 2013, 19, 2271-2274.
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35
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V. Schmidts, M. Fredersdorf, T. Lübken, A. Porzel, N. Arnold, L. Wessjohann, C. M. Thiele, RDC-Based Determination of the Relative Configuration of the Fungicidal Cyclopentenone 4,6-Diacetylhygrophorone A12, J. Nat. Prod. 2013, 76, 839-844.
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36
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A. Kolmer, L. Kaltschnee, V. Schmidts, L. H. Peeck, H. Plenio, C. M. Thiele, The influence of electronic modifications on rotational barriers of bis-NHC-complexes as observed by dynamic NMR spectroscopy, Magn. Reson. Chem. 2013, 51, 695–700.
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37
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V. Thiel, K.-J. Wannowius, C. Wolff, C. M. Thiele, H. Plenio, Ring-Closing Metathesis Reactions: Interpretation of Conversion–Time Data, Chem. Eur. J. 2013, 19, 16403–16414.
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38
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I. Timári, L. Kaltschnee, A. Kolmer, R. W. Adams, M. Nilsson, C. M. Thiele, G. A. Morris, K. E. Kövér, Accurate determination of one-bond heteronuclear coupling constants with “pure shift” broadband proton-decoupled CLIP/CLAP-HSQC experiments, J. Magn. Reson. 2014, 239, 130-138.
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39
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L. Kaltschnee, A. Kolmer, I. Timári, V. Schmidts, R. W. Adams, M. Nilsson, K. E Kövér, G. A Morris, C. M. Thiele, „Perfecting“ pure shift HSQC: full homodecoupling for accurate and precise determination of heteronuclear couplings, Chem. Commun. 2014, 50, 15702-15705.
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40
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B. Horstmann, M. Korbus, T. Friedmann, C. Wolff, C. M. Thiele, F.-J. Meyer-Almes, Synthesis of azobenzenealkylmaleimide probes to photocontrol the enzyme activity of a bacterial histone deacetylase-like amidohydrolase, Bioorg. Chem. 2014, 57, 155-161.
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41
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K. Zhang, A. Geissler, M. Standhardt, S. Mehlhase, M. Gallei, L. Chen, C. M. Thiele, Moisture-responsive films of cellulose stearoyl esters showing reversible shape transitions, Sci. Rep. 2015, 5, 11011.
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42
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L.-G. Xie, V. Bagutski, D. Audisio, L. Wolf, V. Schmidts, K. Hofmann, C. Wirtz, W. Thiel, C. M. Thiele, N. Maulide, Dynamic Behaviour of monohaptoallylpaladium species: internal coordination as a driving force in allylic alkylation chemistry, Chem. Sci. 2015, 6, 5734-5739.
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43
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M. Fredersdorf, R. Göstl, A. Kolmer, V. Schmidts, P. Monecke, S. Hecht, C. M. Thiele, Exploring the Conformational Space of Bridge-Substituted Dithienylcyclopentenes, Chem. Eur. J. 2015, 21, 14545–14554.
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44
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J. Kind, C. M. Thiele, Still shimming or already measuring? – Quantitative reaction monitoring for small molecules on the sub minute timescale by NMR, J. Magn. Reson. 2015, 260, 109-115.
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45
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A. Kolmer, L. J. Edwards, I. Kuprov, C. M. Thiele, Conformational analysis of small organic molecules using NOE and RDC data: A discussion of strychnine and alpha-methylene-gamma-butyrolactone, J. Magn. Reson. 2015, 261, 101-109.
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46
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C. Wolff, J. Kind, H. Schenderlein, H. Bartling, C. Feldmeier, M. Biesalski, R. M. Gschwind, C. M. Thiele, Studies of a photochromic model system using NMR with ex-situ and in-situ irradiation devices, Magn. Reson. Chem. 2016, 54, 485-491.
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47
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N. Kolmer-Anderl, A. Kolmer, C. M. Thiele, M. Rehahn, Exploration of the photodegradation of naphto[2,3-g]quinoxalines and pyrazino[2,3-b]phenazines, Chem. Eur. J. 2016, 22, 5277–5287.
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48
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S. Hansmann, T. Larem (née Montag), C. M. Thiele, Enantiodifferentiating properties of the alignment media PELG and PBLG -- A comparison, Eur. J. Org. Chem. 2016, 7, 1324–1329.
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49
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F. Krohm, J. Kind, R. Savka, M. Alcaraz Janßen, D. Herold, H. Plenio, C. M. Thiele, A. Andrieu-Brunsen, Photochromic spiropyran- and spirooxazine-homopolymers in mesoporous thin films by surface initiated ROMP, J. Mater. Chem. C 2016, 4, 4067-4076 / Corrigendum.
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50
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C. M. Thiele, A. Kolmer, Response to “Comment on „Conformational Analysis of Small Organic Moleucles using NOE and RDC data: A discussion of strychnine and alpha-methylene-gamma-butyrolactone“” by I. A. Khodov, M. G. Kiselev, V. V. Klochkov, S. V. Efimov – or Life is about compromises, J. Magn. Reson. 2016, 266, 69-72.
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51
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C. M. Thiele, A. S. Ulrich, Light flips a membrane-embedded helix, Science 2016, 352, 520. [Full Text][PDF Reprint]
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52
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M. R. M. Koos, G. Kummerlöwe, L. Kaltschnee, C. M. Thiele, B. Luy, CLIP-COSY: A Clean Inphase Experiment for Rapid Acquisition of COSY-type Correlations, Angew. Chem. 2016, 128, 7785-7789, Angew. Chem. Int. Ed. 2016, 55, 7655-7659.
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53
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L. Kaltschnee, K. Knoll, V. Schmidts, R. W. Adams, M. Nilsson, G. A. Morris, C. M. Thiele, Extraction of Distance Restraints from Pure Shift NOE experiments, J. Magn. Reson. 2016, 271, 99-109.
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54
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I. Timári, L. Kaltschnee, M. H. Raics, F. Roth, N. G. A. Bell, R. W. Adams, M. Nilsson, D. Uhrín, G. A. Morris, C. M. Thiele, K. E. Kövér, Real-time broadband proton-homodecoupled CLIP/CLAP-HSQC for automated measurement of heteronuclear one-bond coupling constants, RSC Adv. 2016, 6, 87848-87855.
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55
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J. Kind, L. Kaltschnee, M. Leyendecker, C. M. Thiele, Distinction of trans-cis photoisomers with comparable optical properties in multiple-state photochromic systems – Examining a molecule with three azobenzenes via in situ irradiation NMR, Chem. Commun. 2016, 52, 12506-12509.
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56
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S. Hörner, S. Knauer, C. Uth, M. Jöst, V. Schmidts, H. Frauendorf, C. M. Thiele, O. Avrutina, H. Kolmar, Nanoscale Biodegradable Organic–Inorganic Hybrids for Efficient Cell Penetration and Drug Delivery, Angew. Chem. 2016, 128, 15063-15068, Angew. Chem. Int. Ed. 2016, 55, 14842-14846.
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57
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E. Procházková, A. Kolmer, J. Ilgen, M. Schwab, L. Kaltschnee, M. Fredersdorf, V. Schmidts, R. C. Wende, P. R. Schreiner, C. M. Thiele, Uncovering Key Structural Features of an Enantioselective Peptide-Catalyzed Acylation Utilizing Advanced NMR Techniques, Angew. Chem. 2016, 128, 15986–15991, Angew. Chem. Int. Ed. 2016, 55, 15754–15759.
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58
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C. M. Thiele, Book Review, Csaba Szántay Jr. (Ed.): Anthropic awareness: the human aspects of scientific thinking in NMR spectroscopy and mass spectrometry, Anal. Bioanal. Chem. 2017, 409, 867-868. [Full Text]
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59
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Yu. E. Moskalenko, V. Bagutski, C. M. Thiele, Chemically synthesized and cross-linked PDMS as versatile alignment medium for organic compounds, Chem. Commun. 2017, 53, 95-98. [Inside Front Cover]
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60
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M. Fredersdorf, M. Kurz, A. Bauer, M.-O. Ebert, C. Rigling, L. Lannes, C. M. Thiele, Conformational analysis of an antibacterial cyclodepsipeptide active against M. tuberculosis by a combined ROE and RDC analysis, Chem. Eur. J. 2017, 24, 5729-5735. [Back Cover]
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61
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S. Hansmann, V. Schmidts, C. M. Thiele, Synthesis of Poly-γ-S-2-methylbutyl-L-glutamate and Poly-γ-S 2-methylbutyl-D-glutamate and their Use as Enantiodiscriminating Alignment Media in NMR Spectroscopy, Chem. Eur. J. 2017, 23, 9114-9121.
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62
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M. Leyendecker, N.-C. Meyer, C. M. Thiele, Development of new supramolecular lyotropic liquid crystals and their application as alignment media for organic compounds, Angew. Chem. 2017, 129, 11629-11632, Angew. Chem. Int. Ed. 2017, 56, 11471-11474.
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63
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M. Schwab, D. Herold, C. M. Thiele, Polyaspartates as Thermoresponsive Enantiodifferentiating Helically Chiral Alignment Media for Anisotropic NMR-Spectroscopy, Chem. Eur. J. 2017, 23, 14576-14584.
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64
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S. Ortgies, R. Rieger, K. Rode, K. Koszinowski, J. Kind, C. M. Thiele, J. Rehbein, A. Breder, Mechanistic and Synthetic Investigations on the Dual Selenium-π-Acid/Photoredox Catalysis in the Context of the Aerobic Dehydrogenative Lactonization of Alkenoic Acids, ACS Catal. 2017, 7, 7578-7586.
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65
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J. Ilgen, L. Kaltschnee, C. M. Thiele, A pure shift experiment with increased sensitivity and superior performance for strongly coupled systems, J. Magn. Reson. 2018, 286, 18-29. [JMR Most-read Publication Award in 2018] [Raw Data: DOI 10.23728/b2share.76f2f9e3f53d4fce90e2ac768102c34e]
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66
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E. Procházková, L. Čechová, J. Kind, Z. Janeba, C. M. Thiele, M. Dračínský, Photoswitchable intramolecular hydrogen bonds in 5-phenylazopyrimidines revealed by in-situ irradiation NMR spectroscopy, Chem. Eur. J. 2018, 24, 492-498.
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67
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S. Fräbel, B. Wagner, M. Krischke, V. Schmidts, C. M. Thiele, A. Staniek, H. Warzecha, Engineering of new-to-nature halogenated indigo precursors in plants, Metab. Eng. 2018, 46, 20-27.
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68
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L. Čechová, J. Kind, M. Dračínský, J. Filo, Z. Janeba, C. M. Thiele, M. Cigáň, E. Procházková, Photoswitching behavior of 5-phenylazopyrimidines: in situ irradiation NMR and optical spectroscopy combined with theoretical methods, J. Org. Chem. 2018, 83, 5986-5998.
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69
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A.-K. Schönbein, J. Kind, C. M. Thiele, J. J. Michels, Full Quantification of the Light-Mediated Gilch Polymerization, Macromolecules 2018, 51, 4678-4687.
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70
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J. Ilgen, L. Kaltschnee, C. M. Thiele, perfectBASH: Band-selective homonuclear decoupling in peptides and peptidomimetics, Magn. Reson. Chem. 2018, 56, 918-933. [Raw Data: DOI 10.23728/b2share.688901f6e4fe4b92bd0238715c3186bb]
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71
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S. Weißheit, M. Kahse, K. Kämpf, A. Tietze, M. Vogel, R. Winter, C. M. Thiele, Elastin-like Peptide in Confinement: FT-IR and NMR T1 Relaxation Data, Z. Phys. Chem. 2018, 232, 1239-1261.
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72
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M. Schwab, V. Schmidts, C. M. Thiele, Thermoresponsive Alignment Media in NMR spectroscopy: Helix Reversal of a Copolyaspartate at Ambient Temperatures, Chem. Eur. J. 2018, 24, 14373-14377.
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73
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S. Jeziorowski, C. M. Thiele, Poly‐γ‐p‐biphenylmethyl‐glutamate as Enantiodifferentiating Alignment Medium for NMR‐Spectroscopy with Temperature Tunable Properties, Chem. Eur. J. 2018, 24, 15631-15637.
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74
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K. Knoll, M. Leyendecker, C. M. Thiele, L‐Valine derivatised 1,3,5‐Benzene‐tricarboxamides as Building Blocks for a new Supramolecular Organogel‐like Alignment Medium, Eur. J. Org. Chem. 2019, 2019, 720-727.
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75
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A. Matt, B. Kuttich, I. Grillo, S. Weißheit, C. M. Thiele, B. Stühn, Temperature induced conformational changes in the elastin-like peptide GVG(VPGVG)3, Soft Matter 2019, 15, 4192-4199.
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76
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Y. Ji, D. DiRocco, J. Kind, C. M. Thiele, R. M. Gschwind, M. Reibarkh, LED Illuminated NMR spectroscopy: Practical Tool for Mechanistic Studies of Photochemical Reactions, ChemPhotoChem 2019, 3, 984-992.
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77
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M. Hirschmann, M. Schwab, C. M. Thiele, Molecular Weights: The Key for Lyotropic Liquid Crystalline Phases of Poly-β-benzyl-L-aspartate, Macromolecules 2019, 52, 6025-6034.
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78
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J. Kind,* C. M. Thiele, MRI and localised NMR spectroscopy of sessile droplets on hydrophilic,hydrophobic and superhydrophobic surfaces – Examination of thechemical composition during evaporation, J. Magn. Reson. 2019, 307, 106579. [Raw Data: DOI 10.23728/b2share.5f4f0b7ae6d84ab8bdab95131d6ed0a3]
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79
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J. von Irmer, F. Frieß, D. Herold, J. Kind, C. M. Thiele, M. Gallei, Photochromic Dithienylethenes Characterized by in situ Irradiation NMR-Spectroscopy and Electrochemically-Induced Responsiveness on Gold Substrates, J. Mater. Chem. C 2019, 7, 14088-14097.
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80
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D. Niedek, F. R. Erb, C. Topp, A. Seitz, R. C. Wende, A. K. Eckhardt, J. Kind, D. Herold, C. M. Thiele, P. R. Schreiner, In situ Switching of Site-Selectivity with Light in the Acetylation of Sugars with Azo-Peptide Catalysts, J. Org. Chem. 2020, 85, 1835-1846.
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81
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D. Sinnaeve, J. Ilgen, M. E. Di Pietro, J. J. Primozic, V. Schmidts, C. M. Thiele, B. Luy, Probing long-range anisotropic interactions – A general and sign-sensitive strategy to measure 1H-1H residual dipolar couplings as a key advance for organic structure determination, Angew. Chem. Int. Ed. 2020, 59, 5316-5320; Angew. Chem. 2020, 132, 5354-5358. [Raw Data: DOI 10.6084/m9.figshare.11297651]
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82
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M. Alcaraz Janßen, C. M. Thiele, Poly‐γ‐S‐perillyl‐L‐glutamate and Poly‐γ‐S‐perillyl‐D‐glutamate: diastereomeric alignment media used for the investigation of the alignment process, Chem. Eur. J. 2020, 26, 7831-7839.
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83
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P. Weigl,* D. Schadt, S. Weißheit, C. M. Thiele, T. Walther, T. Blochowicz, Triplet state solvation dynamics: extending the accessible timescale by using indole as local probe, Phys. Chem. Chem. Phys. 2021, 23, 683-693.
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84
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J. Ilgen, J. Nowag, L. Kaltschnee, V. Schmidts, C. M. Thiele, Gradient Selected Pure-Shift EASY-ROESY techniques facilitate the quantitative measurement of 1H,1H-distance restraints in congested spectral regions, J. Magn. Reson. 2021, 324, 106900. [Preprint: PDF | SI] [Free Access: PDF]
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85
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M. Hirschmann, C. Merten, C. M. Thiele, Treating Anisotropic Artefacts in Circular Dichroism Spectroscopy Enables Investigation of Lyotropic Liquid Crystalline Polyaspartate Solutions, Soft Matter 2021, 17, 2849-2856.
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86
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M. Hirschmann, D. S. Schirra, C. M. Thiele, Copolyaspartates: Uncovering Simultaneous Thermo and Magnetoresponsiveness, Macromolecules 2021, 54, 1648-1656.
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