Recent advances in subphthalocyanines and related subporphyrinoids
Half a century after the synthesis of the first subporphyrinoid, the study of tripyrrole and
trisoindole porphyrin analogues constitutes a fervent and rapidly expanding research area …
trisoindole porphyrin analogues constitutes a fervent and rapidly expanding research area …
Azadipyrromethenes: from traditional dye chemistry to leading edge applications
Y Ge, DF O'Shea - Chemical Society Reviews, 2016 - pubs.rsc.org
Azadipyrromethenes were first described over 70 years ago as blue pigments, but now are
rapidly emerging as a compound class with highly desirable near infrared photophysical …
rapidly emerging as a compound class with highly desirable near infrared photophysical …
Triplet–triplet annihilation upconversion kinetics of C 60–Bodipy dyads as organic triplet photosensitizers
Three new triplet photosensitizers consisting of a bodipy derivative and C60 moieties were
synthesized for triplet–triplet annihilation upconversion of perylene. With the extension of the …
synthesized for triplet–triplet annihilation upconversion of perylene. With the extension of the …
Donor-acceptor architectures of tetraphenylethene linked aza-BODIPYs: Synthesis, crystal structure, energy transfer and computational studies
This work is focused on the design and synthesis of donor-acceptor pairs comprising of aza-
BODIPY and tetraphenylethene (TPE) fluorogens with large pseudo Stokes shifts (386–424 …
BODIPY and tetraphenylethene (TPE) fluorogens with large pseudo Stokes shifts (386–424 …
Controlling the optical properties of boron subphthalocyanines and their analogues
M Dowds, MB Nielsen - Molecular Systems Design & Engineering, 2021 - pubs.rsc.org
Boron subphthalocyanines (SubPcs) are cone shaped π-conjugated molecules comprised
of three azomethine-bridged isoindole units and a central boron atom with an axial …
of three azomethine-bridged isoindole units and a central boron atom with an axial …
Synthesis of a dual clickable fullerene platform and construction of a dissymmetric BODIPY-[60] Fullerene-DistyrylBODIPY triad
J Rabah, L Yonkeu, K Wright, A Vallée… - Tetrahedron, 2021 - Elsevier
The synthesis of a methanofullerene platform bearing on one side an alkyne and on the
other a protected alkyne is reported. This clickable fullerene building block was …
other a protected alkyne is reported. This clickable fullerene building block was …
Photoactive preorganized subphthalocyanine-based molecular tweezers for selective complexation of fullerenes
G Zango, M Krug, S Krishna, V Mariñas, T Clark… - Chemical …, 2020 - pubs.rsc.org
The development of new chromophoric receptors capable of binding curved carbon
nanostructures is central to the quest for improved fullerene-based organic photovoltaics …
nanostructures is central to the quest for improved fullerene-based organic photovoltaics …
Efficient electron transporting and panchromatic absorbing FRET cassettes based on aza-BODIPY and perylenediimide towards multiple metal FRET-Off sensing and …
K Rani, UK Pandey, S Sengupta - Journal of Materials Chemistry C, 2021 - pubs.rsc.org
Multichromophoric triads 1 and 2 based on aza-BODIPY as the central chromophore and
bay-substituted (tetrachloro-and tetraphenoxy-) perylenediimides (PDI) as peripheral …
bay-substituted (tetrachloro-and tetraphenoxy-) perylenediimides (PDI) as peripheral …
Photoinduced electron transfer and unusual environmental effects in fullerene–Zn-porphyrin–BODIPY triads
Molecular arrays containing donor–acceptor sites and antenna molecules are promising
candidates for organic photovoltaic devices. Photoinduced electron transfer (PET) in multi …
candidates for organic photovoltaic devices. Photoinduced electron transfer (PET) in multi …
Directly Attached Bisdonor‐BF2 Chelated Azadipyrromethene‐Fullerene Tetrads for Promoting Ground and Excited State Charge Transfer
MA Collini, MB Thomas, V Bandi… - … A European Journal, 2017 - Wiley Online Library
The efficiency and mechanism of electron‐and energy‐transfer events occurring in both
natural and synthetic donor–acceptor systems depend on their distance, relative orientation …
natural and synthetic donor–acceptor systems depend on their distance, relative orientation …