Startseite Complete NMR assignment and analysis of molecular structural changes of β–O–4 lignin oligomer model compounds in organic media with different water content
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Complete NMR assignment and analysis of molecular structural changes of β–O–4 lignin oligomer model compounds in organic media with different water content

  • Yuki Tokunaga , Takashi Nagata , Keiko Kondo , Masato Katahira und Takashi Watanabe EMAIL logo
Veröffentlicht/Copyright: 28. August 2020
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Abstract

The conformation of lignin in solvents is major key factors governing the physicochemical properties of aromatic polymers. However, the conformational changes of lignin in good and poor solvents is not clearly understood at the molecular level. In this study, short- (DP 2.77) and long-chain (DP 4.49) lignin oligomer model compounds composed solely of interunit β–O–4 bonds with a narrow polydispersity were synthesized, and their NMR spectra were recorded to evaluate the molecular structural changes induced by addition of water to an organic solvent. The spectral signals were completely assigned in DMSO-d6 and D2O by applying 2D 1H–13C HSQC, HMBC, and long-range heteronuclear single quantum multiple bond correlation (LR-HSQMBC). The conformation of the long- and short-chain lignin models were analyzed by 2D 1H–1H ROESY. In all the solvent systems, consisting of DMSO-d6 and containing 0–90% volume of acetic acid-d4 buffer in D2O (pD 5.0), the lignin models were found to have folded conformations, but more compact structures were observed in D2O compared with DMSO-d6.


Corresponding author: Takashi Watanabe, Research Institute for Sustainable Humanosphere (RISH), Kyoto University, Uji 611-0011, Japan, E-mail:

Award Identifier / Grant number: Kakenhi JP18J20331

Funding source: Research Institute of Sustainable Humanosphere, Kyoto University

Award Identifier / Grant number: Collaboration program of RISH M2-2

Funding source: Institute of Advanced Energy, Kyoto University

Award Identifier / Grant number: Joint usage/Research Programs of IAE ZE30A-36, Z

  1. Author contribution: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This work was supported by JSPS KAKENHI grant number JP18J20331, a collaboration program of RISH (M2-2) and joint usage/research program of IAE (ZE30A-36, ZE31A-37).

  3. Conflict of interest statement: The authors declare no conflicts of interest regarding this article.

References

Abbati de Assis, C., Greca, L.G., Ago, M., Balakshin, M.Y., Jameel, H., Gonzalez, R., and Rojas, O.J. (2018). Techno-economic assessment, scalability, and applications of aerosol lignin micro- and nanoparticles. ACS Sustain. Chem. Eng. 6: 11853–68, https://doi.org/10.1021/acssuschemeng.8b02151.Suche in Google Scholar

Bardet, M., Robert, D., Lundquist, K., and von Unge, S. (1998). Distribution of erythro and threo forms of different types of β-O-4 structures in aspen lignin by 13C NMR using the 2D INADEQUATE experiment. Mgn. Reson. Chem. 36: 597–600, https://doi.org/10.1002/(sici)1097-458x(199808)36:8%3c;597::aid-omr345%3e;3.0.co;2-g.10.1002/(SICI)1097-458X(199808)36:8<597::AID-OMR345>3.0.CO;2-GSuche in Google Scholar

Besombes, S., Utille, J.P., Mazeau, K., Robert, D., and Taravel, F.R. (2004). Conformational study of a guaiacyl beta-O-4 lignin model compound by NMR. Examination of intramolecular hydrogen bonding interactions and conformational flexibility in solution. Magn. Reson. Chem. 42: 337–47, https://doi.org/10.1002/mrc.1317.Suche in Google Scholar

Crestini, C., Melone, F., Sette, M., and Saladino, R. (2011). Milled wood lignin: a linear oligomer. Biomacromolecules 12: 3928–35, https://doi.org/10.1021/bm200948r.Suche in Google Scholar

Ding, R., Wu, H., Thunga, M., Bowler, N., and Kessler, M.R. (2016). Processing and characterization of low-cost electrospun carbon fibers from organosolv lignin/polyacrylonitrile blends. Carbon 100: 126–36, https://doi.org/10.1016/j.carbon.2015.12.078.Suche in Google Scholar

Fritz, C., Salas, C., Jameel, H., and Rojas, O.J. (2017). Self-association and aggregation of kraft lignins via electrolyte and nonionic surfactant regulation: stabilization of lignin particles and effects on filtration - OPEN ACCESS. Nord. Pulp Pap Res. J. 32: 572–585, https://doi.org/10.3183/npprj-2017-32-04_p572-585_rojas.Suche in Google Scholar

Garver, T.M., Maa, K.J., and Marat, K. (1996). Conformational analysis and 2D NMR assignment strategies for lignin model compounds. The structure of acetoguaiacyl-dehydro-diisoeugenol methyl ether. Canadian Journal of Chemistry-Revue Canadienne De Chimie 74: 173–84, https://doi.org/10.1139/v96-021.Suche in Google Scholar

Kaiho, A., Mazzarella, D., Satake, M., Kogo, M., Sakai, R., and Watanabe, T. (2016). Construction of the di(trimethylolpropane) cross linkage and the phenylnaphthalene structure coupled with selective beta-O-4 bond cleavage for synthesizing lignin-based epoxy resins with a controlled glass transition temperature. Green Chem. 18: 6526–35, https://doi.org/10.1039/c6gc02211a.Suche in Google Scholar

Katahira, R., Kamitakahara, H., Takano, T., and Nakatsubo, F. (2006). Synthesis of β-O-4 type oligomeric lignin model compound by the nucleophilic addition of carbanion to the aldehyde group. J. Wood Sci. 52: 255–60, https://doi.org/10.1007/s10086-005-0756-1.Suche in Google Scholar

Kishimoto, T., Uraki, Y., and Ubukata, M. (2008). Synthesis of beta-O-4-type artificial lignin polymers and their analysis by NMR spectroscopy. Org. Biomol. Chem. 6: 2982–7, https://doi.org/10.1039/b805460f.Suche in Google Scholar

Lancefield, C.S., Ojo, O.S., Tran, F., and Westwood, N.J. (2015). Isolation of functionalized phenolic monomers through selective oxidation and C-O bond cleavage of the beta-O-4 linkages in lignin. Angew Chem. Int. Ed. Engl. 54: 258–62, https://doi.org/10.1002/anie.201409408.Suche in Google Scholar

Lievonen, M., Valle-Delgado, J.J., Mattinen, M.-L., Hult, E.-L., Lintinen, K., Kostiainen, M.A., Paananen, A., Szilvay, G.R., Setälä, H., and Österberg, M. (2016). A simple process for lignin nanoparticle preparation. Green Chem. 18: 1416–22, https://doi.org/10.1039/c5gc01436k.Suche in Google Scholar

Petridis, L., and Smith, J.C. (2016). Conformations of low-molecular-weight lignin polymers in water. ChemSusChem 9: 289–95, https://doi.org/10.1002/cssc.201501350.Suche in Google Scholar

Ralph, J., Marita, J.M., Ralph, S.A., Hatfield, R.D., Lu, F., Ede, R.M., Peng, J., and Landucci, L.L. (1999). Solution state NMR of lignins. In: Atlanta, G. (Ed.), Advances in lignocellulosics characterization: TAPPI Press, pp. 55–108.Suche in Google Scholar

Robert, E.I., Richard, H.M., and Alvin, K.W. (1976). The ester enolate claisen rearrangement. Stereochemical control through stereoselective enolate formation. J. Am. Chem. Soc. 98: 2868–77.10.1021/ja00426a033Suche in Google Scholar

Silveira, R.L., Stoyanov, S.R., Gusarov, S., Skaf, M.S., and Kovalenko, A. (2015). Supramolecular interactions in secondary plant cell walls: effect of lignin chemical composition revealed with the molecular theory of solvation. J. Phys. Chem. Lett. 6: 206–11, https://doi.org/10.1021/jz502298q.Suche in Google Scholar

Sipponen, M.H., Lange, H., Ago, M., and Crestini, C. (2018). Understanding lignin aggregation processes. A case study: budesonide entrapment and stimuli controlled release from lignin nanoparticles. ACS Sustain. Chem. Eng. 6: 9342–51, https://doi.org/10.1021/acssuschemeng.8b01652.Suche in Google Scholar

Spiridon, I., Leluk, K., Resmerita, A.M., and Darie, R.N. (2015). Evaluation of PLA–lignin bioplastics properties before and after accelerated weathering. Compos. B Eng. 69: 342–9, https://doi.org/10.1016/j.compositesb.2014.10.006.Suche in Google Scholar

Stockmayer, W.H. (1960). Problems of the statistical thermodynamics of dilute polymer solutions. Makromol. Chem. 35: 54–74, https://doi.org/10.1002/macp.1960.020350103.Suche in Google Scholar

Tokunaga, Y., Nagata, T., Suetomi, T., Oshiro, S., Kondo, K., Katahira, M., and Watanabe, T. (2019). NMR Analysis on molecular interaction of lignin with amino acid residues of carbohydrate-binding module from Trichoderma reesei Cel7A. Sci. Rep. 9: 1977, https://doi.org/10.1038/s41598-018-38410-9.Suche in Google Scholar

Williamson, R.T., Buevich, A.V., Martin, G.E., and Parella, T. (2014). LR-HSQMBC: a sensitive NMR technique to probe very long-range heteronuclear coupling pathways. J. Org. Chem. 79: 3887–94, https://doi.org/10.1021/jo500333u.Suche in Google Scholar

Yanase, Y., Sakamoto, K., and Imai, T. (2015). Isolation and structural elucidation of norlignan polymers from the heartwood of Cryptomeria japonica. Holzforschung 69: 281–296, https://doi.org/10.1515/hf-2013-0251.Suche in Google Scholar

Yang, Y.N., Huang, X.Y., Feng, Z.M., Jiang, J.S., and Zhang, P.C. (2015). New butyrolactone type lignans from arctii fructus and their anti-inflammatory activities. J. Agric. Food Chem. 63: 7958–66, https://doi.org/10.1021/acs.jafc.5b02838.Suche in Google Scholar

Yu, J., Wang, J., Wang, C., Liu, Y., Xu, Y., Tang, C., and Chu, F. (2015). UV-absorbent lignin-based multi-arm star thermoplastic elastomers. Macromol. Rapid Commun. 36: 398–404, https://doi.org/10.1002/marc.201400663.Suche in Google Scholar

Zhao, W., Xiao, L.-P., Song, G., Sun, R.-C., He, L., Singh, S., Simmons, B.A., and Cheng, G. (2017). From lignin subunits to aggregates: insights into lignin solubilization. Green Chem. 19: 3272–3281, https://doi.org/10.1039/c7gc00944e.Suche in Google Scholar

Supplementary material

The online version of this article offers supplementary material (https://doi.org/10.1515/hf-2020-0039).

Received: 2020-03-19
Accepted: 2020-07-14
Published Online: 2020-08-28
Published in Print: 2021-04-27

© 2020 Walter de Gruyter GmbH, Berlin/Boston

Heruntergeladen am 2.12.2025 von https://www.degruyterbrill.com/document/doi/10.1515/hf-2020-0039/pdf
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