A cyclic complex [Ni(12)(chp)(12)(O(2)CMe)(12)(thf)(6)(H(2)O)(6)] (1) has been synthesised and studied (chp=6-chloro-2-pyridonate). Complex 1 exhibits ferromagnetic exchange between the S=1 centres, giving an S=12 spin ground state. Detailed studies demonstrate that it is a single-molecule magnet wi
Single-Molecule Studies of a Model Fluorenone
✍ Scribed by Michael Y. Odoi; Nathan I. Hammer; Hemali P. Rathnayake; Paul M. Lahti; Michael D. Barnes
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 316 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1439-4235
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Single‐molecule fluorescence measurements of 2,7‐bis(3,4,5‐trimethoxyphenylethenyl)fluorenone (OFOPV) reveal narrow emission spectra concentrated around 540 nm, with weak emission at longer wavelengths. The wide scattering of emission‐maximum wavelengths is attributed to varying molecular environments, with dimers or higher‐order aggregates contributing to the low‐energy emission. This spectral distribution indicates that emission from monomers of this model fluorenone is mostly green, which is consistent with contaminant emission (g‐bands) often observed in fluorene‐ and polyfluorene‐based organic light emitting diode (OLED) devices. A histogram of center wavelengths from 118 single‐molecule spectra shows good agreement with the green emission previously observed in thermally stressed 2,7‐bis(3,4,5‐trimethoxyphenylethenyl)‐9,9‐diethylfluorene (OFPV). Whereas bulk OFPV exhibits blue fluorescence at about 480 nm, OFOPV bulk thin film measurements reveal red luminescence shifted to 630 nm. This unexpected peak position for bulk OFOPV shifts to higher energies (ca. 540 nm) upon dilution in a solid‐state matrix, suggesting that the bulk red emission finds its origins in interactions between fluorenone molecules. Explanations for this red emission include aggregate or excimer formation or intermolecular energy transfer between fluorenone molecules.
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