0000000000141462

AUTHOR

Peter Sieger

showing 3 related works from this author

Generalized synthesis of periodic surfactant/inorganic composite materials

1994

THE recent synthesis of silica-based mesoporous materials1,2 by the cooperative assembly of periodic inorganic and surfactant-based structures has attracted great interest because it extends the range of molecular-sieve materials into the very-large-pore regime. If the synthetic approach can be generalized to transition-metal oxide mesostructures, the resulting nanocomposite materials might find applications in electrochromic or solid-electrolyte devices3,4, as high-surface-area redox catalysts5 and as substrates for biochemical separations. We have proposed recently6 that the matching of charge density at the surfactant/inorganic interfaces governs the assembly process; such co-organizatio…

chemistry.chemical_classificationchemistry.chemical_compoundMultidisciplinaryNanocompositePulmonary surfactantchemistryElectrochromismOxideCationic polymerizationCounterionComposite materialMesoporous materialElectrostaticsNature
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Organization of Organic Molecules with Inorganic Molecular Species into Nanocomposite Biphase Arrays

1994

chemistry.chemical_classificationNanocompositeChemistryGeneral Chemical EngineeringCarboxylic acidInorganic chemistryGeneral ChemistryPhosphateMicellechemistry.chemical_compoundSulfonateLiquid crystalX-ray crystallographyMaterials ChemistryInorganic compoundChemistry of Materials
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The azulene scaffold from a medicinal chemist's perspective: Physicochemical and in vitro parameters relevant for drug discovery.

2022

Azulene is a bicyclic scaffold rarely applied in medicinal chemistry. Here we report physicochemical and in vitro parameters relevant for drug discovery for a series of diversely substituted azulenes. We synthesized and characterized several scaffold hopping series of analogously substituted azulenes, indoles and naphthalenes. This enabled a comparison of azulene with the more common scaffolds indole and naphthalene. Our data indicates that undesirably low photostability of azulenes is restricted to certain substitution patterns. Generally, we conclude that azulene is an underused lipophilic bicycle and should be considered as a valuable complement to the collection of medicinal chemistry s…

Pharmacologyaromaattiset yhdisteetScaffold hoppingChemistry PharmaceuticalOrganic ChemistryGeneral MedicineAzuleneslääkesuunnitteluPhotostabilitylääkekemiaIndoleDrug Discoveryatsuleenibiologinen aktiivisuusNaphthaleneEuropean journal of medicinal chemistry
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