6233639
DD6FYCHZ
organic-geochemistry
50
date
title
1
Stegbauer, L.
9
https://www.stegbauerlab.de/test/wp-content/plugins/zotpress/
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Gottschling, K., Stegbauer, L., Savasci, G., Prisco, N.A., Berkson, Z.J., Ochsenfeld, C., Chmelka, B.F., Lotsch, B.V., 2019. Molecular Insights into Carbon Dioxide Sorption in Hydrazone-Based Covalent Organic Frameworks with Tertiary Amine Moieties. Chemistry of Materials 31, 1946–1955.
Stegbauer, L., Zech, S., Savasci, G., Banerjee, T., Podjaski, F., Schwinghammer, K., Ochsenfeld, C., Lotsch, B.V., 2018. Tailor-Made Photoconductive Pyrene-Based Covalent Organic Frameworks for Visible-Light Driven Hydrogen Generation. Advanced Energy Materials 8, 1703278.
Haase, F., Gottschling, K., Stegbauer, L., S. Germann, L., Gutzler, R., Duppel, V., S. Vyas, V., Kern, K., E. Dinnebier, R., V. Lotsch, B., 2017. Tuning the stacking behaviour of a 2D covalent organic framework through non-covalent interactions. Materials Chemistry Frontiers 1, 1354–1361.
Stegbauer, L.M., 2016. Two-dimensional covalent organic frameworks as platforms for renewable enegery and environmental applications (PhD Thesis). lmu.
Stegbauer, L., Hahn, M.W., Jentys, A., Savasci, G., Ochsenfeld, C., Lercher, J.A., Lotsch, B.V., 2015. Tunable Water and CO2 Sorption Properties in Isostructural Azine-Based Covalent Organic Frameworks through Polarity Engineering. Chemistry of Materials 27, 7874–7881.
Hug, S., Stegbauer, L., Oh, H., Hirscher, M., Lotsch, B.V., 2015. Nitrogen-Rich Covalent Triazine Frameworks as High-Performance Platforms for Selective Carbon Capture and Storage. Chemistry of Materials 27, 8001–8010.
Vyas, V.S., Haase, F., Stegbauer, L., Savasci, G., Podjaski, F., Ochsenfeld, C., Lotsch, B.V., 2015. A tunable azine covalent organic framework platform for visible light-induced hydrogen generation. Nature Communications 6, 1–9.
Gammack Yamagata, A.D., Datta, S., Jackson, K.E., Stegbauer, L., Paton, R.S., Dixon, D.J., 2015. Enantioselective Desymmetrization of Prochiral Cyclohexanones by Organocatalytic Intramolecular Michael Additions to α,β-Unsaturated Esters. Angewandte Chemie (International Ed. in English) 54, 4899–4903.
Braml, N.E., Stegbauer, L., Lotsch, B.V., Schnick, W., 2015. Synthesis of Triazine-Based Materials by Functionalization with Alkynes. Chemistry – A European Journal 21, 7866–7873.
Stegbauer, L., Schwinghammer, K., V. Lotsch, B., 2014. A hydrazone-based covalent organic framework for photocatalytic hydrogen production. Chemical Science 5, 2789–2793.
Stegbauer, L., Sladojevich, F., J. Dixon, D., 2012. Bifunctional organo/metal cooperative catalysis with cinchona alkaloid scaffolds. Chemical Science 3, 942–958.
Dixon, D.J., Stegbauer, L., 2001. N-[3, 5-Bis (trifluoromethyl) phenyl]-N′-(9 R)-cinchonan-9-yl-thiourea. Encyclopedia of Reagents for Organic Synthesis.