Rational design of pyrrolopyrrole-aza-BODIPY-based acceptor-donor-acceptor triads for organic photovoltaics application
Rational design of pyrrolopyrrole-aza-BODIPY-based acceptor-donor-acceptor triads for organic photovoltaics application
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Chem. Commun. 2020, 56, 2975-2978.
Pyrrolopyrrole Aza‐BODIPY Analogues as Near‐Infrared Chromophores and Fluorophores: Red‐Shift Effects of Substituents on the Absorption and Emission
Pyrrolopyrrole Aza‐BODIPY Analogues as Near‐Infrared Chromophores and Fluorophores: Red‐Shift Effects of Substituents on the Absorption and Emission
ChemPlusChem 2019, 84, 1648–1652.
Core-Modified Phthalocyanines and Subphthalocyanines: a Synthetic Strategy towards Core-Modification and Novel Properties Arising from the Inner Ring-Expansion
Core-Modified Phthalocyanines and Subphthalocyanines: a Synthetic Strategy towards Core-Modification and Novel Properties Arising from the Inner Ring-Expansion
Macroheterocycles 2015, 8, 332-342.
Highly deformed phthalocyanine as a suitable scaffold for pristine fullerenes
Highly deformed phthalocyanine as a suitable scaffold for pristine fullerenes
CrystEngComm 2013, 15, 3759–3762.
Gold(II) Phthalocyanine Revisited: Synthesis and Spectroscopic Properties of Gold(III) Phthalocyanine and an Unprecedented Ring‐Contracted Phthalocyanine Analogue
Gold(II) Phthalocyanine Revisited: Synthesis and Spectroscopic Properties of Gold(III) Phthalocyanine and an Unprecedented Ring‐Contracted Phthalocyanine Analogue
Chem. Eur. J. 2012, 18, 12404–12410.
meso-Aryl substituted rubyrin and its higher homologues: structural characterization and chemical properties
meso-Aryl substituted rubyrin and its higher homologues: structural characterization and chemical properties
Chem. Eur. J. 2008, 14, 2668–2678.
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