Functional oligothiophenes: molecular design for multidimensional nanoarchitectures and their applications

A Mishra, CQ Ma, P Bauerle - Chemical reviews, 2009 - ACS Publications
Functional Oligothiophenes: Molecular Design for Multidimensional Nanoarchitectures and Their
Applications | Chemical Reviews ACS ACS Publications C&EN CAS Find my institution Log In …

Expanded porphyrins: intriguing structures, electronic properties, and reactivities

S Saito, A Osuka - Angewandte Chemie International Edition, 2011 - Wiley Online Library
The chemistry of expanded porphyrins, which are higher homologues of porphyrins, has
been intensively explored for the last three decades. Expanded porphyrins exhibit …

Synthetic expanded porphyrin chemistry

JL Sessler, D Seidel - Angewandte Chemie International …, 2003 - Wiley Online Library
Expanded porphyrins are synthetic analogues of the porphyrins, and differ from these and
other naturally occurring tetrapyrrolic macrocycles by containing a larger central core with a …

Flexible porphyrinoids

B Szyszko, MJ Białek, E Pacholska-Dudziak… - Chemical …, 2017 - ACS Publications
This review underscores the conformational flexibility of porphyrinoids, a unique class of
functional molecules, starting from the smallest triphyrins (1.1. 1) via [18] porphyrins (1.1 …

Topology in chemistry: designing Möbius molecules

R Herges - Chemical reviews, 2006 - ACS Publications
In 1747, Johann Sebastian Bach wrote a series of canons and fugues on the occasion of his
visit to King Frederick the Great of Prussia in Potsdam. His music of homage, the …

Core-modified expanded porphyrins: new generation organic materials

TK Chandrashekar, S Venkatraman - Accounts of chemical …, 2003 - ACS Publications
Even though the first expanded porphyrin was reported in the mid-1960s, the advances in its
chemistry are more recent. New and powerful synthetic methods have facilitated the …

Structural diversity in expanded porphyrins

R Misra, TK Chandrashekar - Accounts of chemical research, 2008 - ACS Publications
Inspired by the chemistry of porphyrins, in the last decade, a new research area where
porphyrin analogues such as expanded, isomeric, and contracted porphyrins have been …

A near-infrared-fluorescent chemodosimeter for mercuric ion based on an expanded porphyrin

XJ Zhu, ST Fu, WK Wong, JP Guo… - Angewandte Chemie …, 2006 - research.polyu.edu.hk
Abstract (Chemical Equation Presented) Running rings around mercuric ions: A [26]
hexaphyrin (1.1. 1.1. 1.0), comprising an α, α′-bipyrrole unit and four pyrrolic and five …

Expanded porphyrins: functional photoacoustic imaging agents that operate in the NIR-II region

J Chen, AC Sedgwick, S Sen, Y Ren, Q Sun… - Chemical …, 2021 - pubs.rsc.org
Photoacoustic imaging (PAI) relies on the use of contrast agents with high molar absorptivity
in the NIR-I/NIR-II region. Expanded porphyrins, synthetic analogues of natural tetrapyrrolic …

Synthesechemie expandierter Porphyrine

JL Sessler, D Seidel - Angewandte Chemie, 2003 - Wiley Online Library
Abstract Expandierte Porphyrine sind synthetische Analoga der Porphyrine und
unterscheiden sich von diesen und anderen natürlichen makrocyclischen Tetrapyrrolen …