Deep Green

Permanent URI for this collectionhttps://elib.uni-stuttgart.de/handle/11682/12328

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Subject: search.filters.subject.540Institute: search.filters.UBSInstitut.Institut für Polymerchemie

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    Polycondensation‐derived high‐molecular weight lignin as nonblended precursor for carbon fibers
    (2024) Clauss, Manuel M.; Frank, Erik; Bauch, Volker; Kuske, Lisa; Buchmeiser, Michael R.
    A new concept for the controlled chain‐extension of lignin has been developed. A mixture of trioxane as formaldehyde source, resorcinol as chain extender, and lignin allows to prepare high molecular weight precursor fibers by melt‐spinning, which can be spun on a semitechnical scale. Chain extension with resorcinol bridged by methylene groups is achieved during the stabilization process of the precursor fiber. After carbonization, carbon fibers (CFs) with an average diameter of 18 µm show an average tensile strength of 0.78 GPa and a Young's modulus of 106 GPa. A maximum tensile strength of 2.44 GPa and a Young's modulus of 294 GPa are reached with fibers 9.7 µm in diameter.
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    The role of spacer length in macrocyclization reactions under confinement
    (2024) Nandeshwar, Muneshwar; Weisser, Kilian; Ziegler, Felix; Frey, Wolfgang; Buchmeiser, Michael R.
    We studied the influence of the distance of olefin metathesis catalysts from the inner surface of a mesoporous support on macrocyclization and Z‐selectivity under confinement. For these purposes, the cationic molybdenum imido alkylidene N‐heterocyclic carbene (NHC) catalysts [Mo(N‐(2‐tBu‐C6H4)(1‐mesityl‐3‐(3‐trimethoxysilylprop‐1‐yl)‐imidazol‐2‐ylidene)(CHCMe2Ph)(MeCN)Br+ B(ArF)4-] Mo2, [Mo(N‐(2‐tBu‐C6H4)(1‐mesityl‐3‐(3‐trimethoxysilylprop‐1‐yl)‐imidazol‐2‐ylidene)(CHCMe2Ph)(MeCN)OTf+ B(ArF)4-] Mo3, [Mo(N‐(2,6‐Me2‐C6H3)(1‐mesityl‐3‐(3‐trimethoxysilylprop‐1‐yl)‐imidazol‐2‐ylidene)(CHCMe2Ph)(MeCN)Br+ B(ArF)4-] Mo5, and [Mo(N‐(2,6‐iPr2‐C6H3)(1‐mesityl‐3‐(3‐trimethoxysilylprop‐1‐yl)‐imidazol‐2‐ylidene)(CHCMe2Ph)(MeCN)+Br B(ArF)4-] Mo7 (B(ArF)4 = tetrakis[3,5‐bis(trifluoromethyl)phenyl]borate), all containing a trimethoxysilylpropyl tether, were selectively immobilized inside the mesopores of SBA‐15. Under confinement, both macro(mono)cyclization (MMC) and Z‐selectivity were higher than in solution but lower than with catalysts directly bound to the surface of the mesoporous supports. These findings are in agreement with existing theoretical models on substrate and product distribution in mesopores, which suggest that the highest substrate concentration is found at the pore wall and that it increases with decreasing pore diameter.