[HTML][HTML] Supramolecular self-assemblies as functional nanomaterials

E Busseron, Y Ruff, E Moulin, N Giuseppone - Nanoscale, 2013 - pubs.rsc.org
In this review, we survey the diversity of structures and functions which are encountered in
advanced self-assembled nanomaterials. We highlight their flourishing implementations in …

Optically active porphyrin and phthalocyanine systems

H Lu, N Kobayashi - Chemical reviews, 2016 - ACS Publications
This review highlights and summarizes various optically active porphyrin and
phthalocyanine molecules prepared using a wide range of structural modification methods …

Porphyrin-based sensor nanoarchitectonics in diverse physical detection modes

S Ishihara, J Labuta, W Van Rossom… - Physical Chemistry …, 2014 - pubs.rsc.org
Porphyrins and related families of molecules are important organic modules as has been
reflected in the award of the Nobel Prizes in Chemistry in 1915, 1930, 1961, 1962, 1965 …

Wraparound hosts for fullerenes: tailored macrocycles and cages

D Canevet, EM Pérez, N Martín - … Chemie International Edition, 2011 - Wiley Online Library
Custom‐made macrocyclic receptors for fullerenes are proving a valuable alternative to
achieve the affinity and selectivity required to meet challenges such as the selective …

Transient helicity: fuel‐driven temporal control over conformational switching in a supramolecular polymer

S Dhiman, A Jain, SJ George - Angewandte Chemie, 2017 - Wiley Online Library
Synthetic manifestations of supramolecular chirality have extensively drawn inspiration from
naturally occurring systems. Even though in biological systems conformational changes are …

A voyage into the synthesis and photophysics of homo-and heterobinuclear ensembles of phthalocyanines and porphyrins

G de la Torre, G Bottari, M Sekita… - Chemical Society …, 2013 - pubs.rsc.org
The remarkable properties of both phthalocyanines and porphyrins as individual building
blocks have motivated the synthesis and study of homo-and heterobinuclear conjugates as …

Macrocyclic hosts for fullerenes: extreme changes in binding abilities with small structural variations.

D Canevet, M Gallego, H Isla, A de Juan… - Journal of the …, 2011 - ACS Publications
Exploiting the shape and electronic complementarity of C60 and C70 with π-extended
derivatives of tetrathiafulvalene (exTTF), we have very recently reported a macrocyclic …

Cyclic metalloporphyrin dimers: Conformational flexibility, applications and future prospects

P Mondal, SP Rath - Coordination Chemistry Reviews, 2020 - Elsevier
Over the past few decades, cyclic metalloporphyrin dimers have been significantly exploited
in the fields of molecular motion, switches, recognition, biomimetic chemistry, and …

Chiroptical and catalytic properties of doubly binaphthyl-strapped chiral porphyrins

C Maeda, K Ogawa, K Sadanaga, K Takaishi… - Chemical …, 2019 - pubs.rsc.org
Doubly (R)-binaphthyl-strapped porphyrins with methylene chains were synthesized. The
CD spectra showed the positive Cotton effect around the Soret bands, and several …

Phosphorus-containing chiral molecule for fullerene recognition based on concave/convex interaction

M Yamamura, T Saito, T Nabeshima - Journal of the American …, 2014 - ACS Publications
AC 3-symmetric chiral concave molecule having a phosphorus atom at the center was
synthesized, and its enantiomers were resolved. The chiral concave shape and absolute …