domain (head) of the surfactant influence the cmc. The two Relationships between the molecular structure and the critical contributions are counteracting, with a lower cmc for a larger micelle concentration (cmc) of anionic surfactants were investihydrophobic domain and a higher cmc for a larger hyd
Quantitative Structure-Fluorescence Property Relationship Analysis of a Large BODIPY Library
✍ Scribed by Andreas Schüller ; Garrett Benjamin Goh; Hanjo Kim ; Jun-Seok Lee; Young-Tae Chang
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Tongue
- English
- Weight
- 447 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1868-1743
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A quantitative structure‐fluorescence property relationship (QSPR) analysis of a large 288‐membered library based on a single fluorescent BODIPY scaffold is presented for the first time. BODIPY is a versatile fluorescent scaffold with outstanding photophysical properties. Absorption (λ~abs~) and fluorescence emission (λ~em~) wavelength maxima were modeled with help of stepwise multiple linear regression (MLR) and support vector regression (SVR). The models were rigorously validated by 10‐times 10‐fold cross‐validation (CV), y‐scrambling CV and with an external validation set. Non‐linear SVR models (R^2^=0.92 and Q^2^=0.71 for λ~abs~; R^2^=0.89 and Q^2^=0.69 for λ~em~) performed significantly better than linear models. A small root mean squared error (RMSE) of 5.62 nm and 11.07 nm was achieved for λ~abs~ and λ~em~, respectively, and confirmed by external validation. A novel intramolecular charge transfer descriptor was developed based on the QSPR analysis and its inclusion in the modeling significantly improved models of λ~em~. We conclude that QSPR is a useful tool for modeling λ~abs~ and λ~em~ of BODIPY fluorophores and suggest QSPR as an ideal partner for the design of compounds with tailored fluorescence properties in a diversity‐oriented fluorescence library approach (DOFLA).
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