RESUMO
We have designed and synthesized three novel twistacene-modified enlarged pentagon-containing π-systems (6 and 9) with mismatched structures. The introduction of electron-withdrawing cyclopenta rings in the parent skeleton effectively stabilizes the electron-rich arenes. Their optoelectronic properties were studied via ultraviolet-visible (UV-vis) absorption spectra, fluorescence spectra, cyclic voltammetry, and density functional theory (DFT) calculation. In addition, chemical oxidation of the as-prepared compounds with nitrosonium hexafluoroantimonate could form the corresponding cationic radicals.
RESUMO
The Nyquist folding receiver (NYFR) can achieve a high-probability interception of an ultra-wideband (UWB) signal with fewer devices, while the output of the NYFR is converted into a hybrid modulated signal of the local oscillator (LO) and the received signal, which requires the matching parameter estimation methods. The linear frequency modulation (LFM) signal is a typical low probability of intercept (LPI) radar signal. In this paper, an estimation method of both the Nyquist Zone (NZ) index and the chirp rate for the LFM signal intercepted by NYFR was proposed. First, according to the time-frequency characteristics of the LFM signal, the accurate NZ and the rough chirp rate was estimated based on least squares (LS) and random sample consensus (RANSAC). Then, the information of the LO was removed from the hybrid modulated signal by the known NZ, and the precise chirp rate was obtained by using the fractional Fourier transform (FrFT). Moreover, a fast search method of FrFT optimal order was presented, which could obviously reduce the computational complexity. The simulation demonstrated that the proposed method could precisely estimate the parameters of the hybrid modulated output signal of the NYFR.
RESUMO
Two novel [5]helicene derivatives (labeled 5 and 8) have been successfully synthesized and characterized. The structural analyses, photophysical properties, along with density functional theory calculations for unveiling the helicity inversion and equilibrium of the diastereomers, were investigated in a comparative manner. In addition, chemical oxidation of them indicated that molecule 8 exhibited the formation of the radical cation at room temperature.