0000000000178641

AUTHOR

Juergen Gerold

showing 3 related works from this author

ChemInform Abstract: Bathochromic or Hypsochromic Effects via the Extension of Conjugation: A Study Stilbenoid Squaraines.

2010

ChemistryBathochromic shiftHypsochromic shiftGeneral MedicineStilbenoidPhotochemistryChemInform
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ChemInform Abstract: Bis-, Tris-, and Tetrakis(squaraines) Linked by Stilbenoid Scaffolds.

2010

The oligosquaraines 1−5, with stilbenoid scaffolds, were prepared by multistep syntheses in which the final steps consisted of condensation reactions between the semisquaric acid 21 and multiple resorcinols 12b−15b and 17b. The target compounds exhibit intense (ϵ > 250000 L·mol−1·cm−1) and sharp absorption bands with maxima between 687 to 778 nm, depending on the conjugation in the stilbenoid scaffold. Comparison with the monosquaraine 6 as a model compound reveals intramolecular interactions between different donor−acceptor−donor moieties, which give rise to increased absorption intensities.

Trischemistry.chemical_compoundchemistryIntramolecular forceGeneral MedicineResorcinolAbsorption (chemistry)StilbenoidCondensation reactionPhotochemistryChemInform
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Bis-, Tris-, and Tetrakis(squaraines) Linked by Stilbenoid Scaffolds

2001

The oligosquaraines 1−5, with stilbenoid scaffolds, were prepared by multistep syntheses in which the final steps consisted of condensation reactions between the semisquaric acid 21 and multiple resorcinols 12b−15b and 17b. The target compounds exhibit intense (ϵ > 250000 L·mol−1·cm−1) and sharp absorption bands with maxima between 687 to 778 nm, depending on the conjugation in the stilbenoid scaffold. Comparison with the monosquaraine 6 as a model compound reveals intramolecular interactions between different donor−acceptor−donor moieties, which give rise to increased absorption intensities.

Trischemistry.chemical_compoundUltraviolet visible spectroscopychemistryIntramolecular forceOrganic ChemistryPolymer chemistryResorcinolPhysical and Theoretical ChemistryAbsorption (chemistry)StilbenoidCondensation reactionPhotochemistryEuropean Journal of Organic Chemistry
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