Publications by authors named "Susanne Seupel"

During the last decades, poly(2-oxazoline)s (POx) have gained increased interest due to their versatility. In particular, cationic ring-opening polymerization (CROP) enables the synthesis of well-defined polymers bearing quantitative α- and ω-functionalities. In contrast to small initiating groups, the introduction of more sophisticated, respectively demanding groups remains challenging.

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Although carbon monoxide (CO) delivery materials (CORMAs) have been generated, remote-controlled delivery with light-activated CORMAs at a local site has not been achieved. In this work, a fiber optic-based CO delivery system is described in which the photoactive and water insoluble CO releasing molecule (CORM) manganese(i) tricarbonyl [(OC)3Mn(μ3-SR)]4 (R = nPr, 1) has been non-covalently embedded into poly(l-lactide-co-d/l-lactide) and poly(methyl methacrylate) non-woven fabrics via the electrospinning technique. SEM images of the hybrid materials show a porous fiber morphology for both polymer supports.

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The amidines Dipp-N=C(tBu)-N(H)-Qu (1a) (Dipp = 2,6-diisopropylphenyl, Qu = 8-quinolyl) and Dipp-N=C(tBu)-N(H)-Py (1b) (Py = 2-pyridyl) are deprotonated with KN(SiMe3)2, yielding potassium N-(2,6-diisopropylphenyl)-N'-(8-quinolyl)pivalamidinate (2a) and potassium N-(2,6-diisopropylphenyl)-N'-(2-pyridyl)pivalamidinate (2b). Metalation of 1a with [(thf)2Ca{N(SiMe3)2}2] in tetrahydrofuran (thf) leads to the formation of ether-free calcium bis[N-(2,6-diisopropylphenyl)-N'-(8-quinolyl)pivalamidinate] (3a) with a strong intramolecular calcium-π interaction with one Dipp group. Furthermore, agostic bonds to one tert-butyl substituent complete the coordination sphere of the metal center and stabilize this bonding situation.

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