[HTML][HTML] Nanostructured artificial photosynthesis

H Imahori, Y Mori, Y Matano - Journal of Photochemistry and Photobiology …, 2003 - Elsevier
We have proposed a novel strategy for artificial photosynthesis where porphyrins and
fullerenes are assembled as building blocks into nanostructured artificial photosynthetic …

Azomethine ylides in organic synthesis

C Najera, JM Sansano - Current Organic Chemistry, 2003 - benthamdirect.com
This review will attempt to cover the literatures published from 1988 dealing with cyclic and
acyclic azomethine ylides in which a part or the whole of the ylide conjugation is included in …

Modulating charge separation and charge recombination dynamics in porphyrin− fullerene linked dyads and triads: Marcus-Normal versus inverted region

H Imahori, K Tamaki, DM Guldi, C Luo… - Journal of the …, 2001 - ACS Publications
Photoinduced charge separation (CS) and charge recombination (CR) processes have
been examined in various porphyrin− fullerene linked systems (ie., dyads and triads) by …

Charge separation in a novel artificial photosynthetic reaction center lives 380 ms

H Imahori, DM Guldi, K Tamaki, Y Yoshida… - Journal of the …, 2001 - ACS Publications
An extremely long-lived charge-separated state has been achieved successfully using a
ferrocene− zincporphyrin− freebaseporphyrin− fullerene tetrad which reveals a cascade of …

Fullerenes: three dimensional electron acceptor materials

DM Guldi - Chemical Communications, 2000 - pubs.rsc.org
This feature article highlights the advantages of employing [60] fullerene as a viable electron
accepting building block in novel donor acceptor systems. Different strategies that aim …

Fullerenes as novel acceptors in photosynthetic electron transfer

H Imahori, Y Sakata - European journal of organic chemistry, 1999 - Wiley Online Library
We propose a novel strategy using fullerenes for the construction of solar energy conversion
systems that mimic the primary electron transfer events in photosynthesis. Redox‐active …

[PDF][PDF] Fullerenes: synthesis and applications

A Nimibofa, EA Newton, AY Cyprain, W Donbebe - J Mater Sci, 2018 - academia.edu
Fullerenes were initially found to be inert, but their unique cage structure and solubility in
organic solvents opened up their susceptibility to functionalization via addition and redox …

Harnessing the synergistic and complementary properties of fullerene and transition-metal compounds for nanomaterial applications

MA Lebedeva, TW Chamberlain… - Chemical …, 2015 - ACS Publications
C60 fullerene is an icosahedrally shaped nanosized molecule and is a useful building block
to form various ordered functional nanostructures due to its size, shape, and …

Vectorial multistep electron transfer at the gold electrodes modified with self-assembled monolayers of ferrocene− porphyrin− fullerene triads

H Imahori, H Yamada, Y Nishimura… - The Journal of …, 2000 - ACS Publications
Self-assembled monolayers of ferrocene− porphyrin− C60 triads on gold electrodes were
prepared to mimic photosynthetic electron transfer events where efficient conversion of light …

Photoinduced electron transfer in carotenoporphyrin− fullerene triads: temperature and solvent effects

D Kuciauskas, PA Liddell, S Lin, SG Stone… - The Journal of …, 2000 - ACS Publications
A carotenoid (C) porphyrin (P) fullerene (C60) molecular triad (C− P− C60) has been
synthesized and found to undergo photoinduced electron transfer from the porphyrin first …