Four different D- and L-configured chromophore–20-deoxyuridine conjugates were applied to elucidate the helical chirality of their non-covalent assemblies along the D- and L-configured DNA templates by optical spectroscopy. There is no configuration-selective recognition between these nucleosides and the DNA templates. The helicity of the DNA assemblies is either controlled by the configuration of the DNA template or by the nucleoside configuration
International audienceTransient or long-term DNA self-assembly participates in essential genetic fun...
The chiral complexes tris(4,7-diphenyl-1,10- phenanthroline)ruthenium(II) (RuDIP) are shown to be s...
Coming together: Oligothymine is used as a template to self-assemble complementary nonchiral naphtha...
Two conjugates of tetraphenylethylene with D-2′-deoxyuridine (1D) and L-2′-deoxyuridine (1L) were sy...
Six different conjugates of perylene with 2′-deoxyuridine and with 2-amino-2′-deoxyadenosine were sy...
DNA was used as supramolecular scaffold to order chromophores and control their optical properties. ...
Cyanolated distyrylbenzene conjugated to 2′-deoxyuridine is a new building block for supramolecular ...
Helicity switching in biological and artificial systems is a fundamental process that allows for the...
Short, complementary DNA single strands with mismatched base pairs cannot undergo spontaneous format...
Chirality plays a primary role in nature and has immense importance in the chemical processes of all...
The use of the DNA duplex as a supramolecular scaffold is an established approach for the assembly o...
The interesting structural, electronic, and optical properties of DNA provide fascinating opportunit...
Concentrated solutions of ultrashort duplex-forming DNA oligomers may develop various forms of liqui...
A chiral dimer of an organic semiconductor was assembled from octaniline (octamer of polyaniline) co...
International audienceTransient or long-term DNA self-assembly participates in essential genetic fun...
The chiral complexes tris(4,7-diphenyl-1,10- phenanthroline)ruthenium(II) (RuDIP) are shown to be s...
Coming together: Oligothymine is used as a template to self-assemble complementary nonchiral naphtha...
Two conjugates of tetraphenylethylene with D-2′-deoxyuridine (1D) and L-2′-deoxyuridine (1L) were sy...
Six different conjugates of perylene with 2′-deoxyuridine and with 2-amino-2′-deoxyadenosine were sy...
DNA was used as supramolecular scaffold to order chromophores and control their optical properties. ...
Cyanolated distyrylbenzene conjugated to 2′-deoxyuridine is a new building block for supramolecular ...
Helicity switching in biological and artificial systems is a fundamental process that allows for the...
Short, complementary DNA single strands with mismatched base pairs cannot undergo spontaneous format...
Chirality plays a primary role in nature and has immense importance in the chemical processes of all...
The use of the DNA duplex as a supramolecular scaffold is an established approach for the assembly o...
The interesting structural, electronic, and optical properties of DNA provide fascinating opportunit...
Concentrated solutions of ultrashort duplex-forming DNA oligomers may develop various forms of liqui...
A chiral dimer of an organic semiconductor was assembled from octaniline (octamer of polyaniline) co...
International audienceTransient or long-term DNA self-assembly participates in essential genetic fun...
The chiral complexes tris(4,7-diphenyl-1,10- phenanthroline)ruthenium(II) (RuDIP) are shown to be s...
Coming together: Oligothymine is used as a template to self-assemble complementary nonchiral naphtha...