about
Integration of inherent and induced chirality into subphthalocyanine analogue.Structurally-modified subphthalocyanines: molecular design towards realization of expected properties from the electronic structure and structural features of subphthalocyanine.Tetrathiafulvalene-annulated subphthalocyanines.A core-expanded subphthalocyanine analogue with a significantly distorted conjugated surface and unprecedented properties.Synthesis of Enantiopure C3 -Symmetric Triangular Molecules.Sizeable red-shift of absorption and fluorescence of subporphyrazine induced by peripheral push and pull substitution.Modified boron subphthalocyanines with stable electrochemistry and tuneable bandgaps.Photoinduced energy and charge transfer in a p-phenylene-linked dyad of boron dipyrromethene and monostyryl boron dipyrromethene.A columnar liquid crystal with permanent polar orderNon-Centrosymmetric Homochiral Supramolecular Polymers of Tetrahedral Subphthalocyanine MoleculesSynthesis and spectroscopic properties of chiral bornane[2,3-b]pyrazino-fused [30]trithiadodecaazahexaphyrinsCyclopentadienylruthenium π Complexes of Subphthalocyanines: A “Drop-Pin” Approach To Modifying the Electronic Features of Aromatic Macrocycles
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description
im November 2011 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 07 October 2011
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в листопаді 2011
@uk
name
Chiral 1,2-Subnaphthalocyanines
@en
Chiral 1,2-Subnaphthalocyanines
@nl
type
label
Chiral 1,2-Subnaphthalocyanines
@en
Chiral 1,2-Subnaphthalocyanines
@nl
prefLabel
Chiral 1,2-Subnaphthalocyanines
@en
Chiral 1,2-Subnaphthalocyanines
@nl
P50
P356
P1476
Chiral 1,2-subnaphthalocyanines
@en
P2093
Akito Miura
Nagao Kobayashi
P304
17322-17328
P356
10.1021/JA2052667
P407
P577
2011-10-07T00:00:00Z