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Cover Picture: Photochromic Organometallics with a Dithienylethene (DTE) Bridge, [YCCDTECCY] (Y={MCp*(dppe)}): Photoswitchable Molecular Wire (M=Fe) versus Dual Photo‐ and Electrochromism (M=Ru) (Chem. Eur. J. 16/2010)
Author(s) -
Tanaka Yuya,
Ishisaka Takuya,
Inagaki Akiko,
Koike Takashi,
Lapinte Claude,
Akita Munetaka
Publication year - 2010
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201090073
Subject(s) - chemistry , photochromism , photoisomerization , molecular switch , photochemistry , triphenylamine , aryl , electrochromism , ruthenium , substituent , acetylide , stereochemistry , isomerization , organic chemistry , molecule , alkyl , catalysis , electrode
The wirelike and switching behavior, as well as the oxidation chemistry, of prepared dinuclear acetylide‐type complexes that are bridged by a photochromic dithienylethene unit (DTE) have been investigated in the Full Paper by M. Akita et al. on page 4762 ff. The photochemical, ring‐opening/closing cycle of the DTE moiety can switch the communication between the two metal centers in the iron complex, and the ruthenium complex exhibits dual photo‐ and electrochromism.

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