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针对公共场所异常声的感知和识别问题,提出一种基于贝叶斯优化卷积神经网络的识别方法。提取声信号的Gammatone倒谱系数、倍频程功率谱、短时能量和谱质心,组合成声信号的特征图。构建卷积神经网络作为分类器,利用递增的卷积核设置和池化操作处理不同尺度的特征。基于贝叶斯优化算法优化卷积神经网络的模型参数,对包括火苗噼啪声、婴儿啼哭声、烟花燃放声、玻璃破碎声和警报声的5种公共场所异常声进行识别。该方法的识别结果与基于不同的特征提取和分类器方案得到的识别结果进行比较,结果表明该方法的识别效果优于其他特征提取和分类器方案的识别效果。最后分析了该方法在不同信噪比噪声干扰下的识别结果,验证了该方法的有效性。 相似文献
34.
This paper seeks to introduce and elaborate on the notion of ‘temporal freedom’ in the context of mathematical thinking.The intention is to merge a philosophical and empirical discussion on this topic, and findings will be presented from a qualitative study in which 29 high-school students were invited to explore the symmetry group of a square during clinical interviews. The data indicate how the interviewees – who were given the opportunity to freely explore an unseen mathematical system – repeatedly brought past and future together in a tangible present during their investigations. In doing so they were exceptionally successful in engaging with advanced abstract algebra, far beyond what might have been expected at the outset.By using empirical data to exemplify an otherwise highly philosophical discussion, I hope to draw explicit attention to the temporal aspect of the human mind in mathematical action which instructional methods frequently fail to recognise, value and utilise. 相似文献
35.
Large‐Scale Synthesis of Enantiopure Molecular Cages: Chiroptical and Recognition Properties 下载免费PDF全文
Sara Lefevre Dawei Zhang Estelle Godart Marion Jean Dr. Nicolas Vanthuyne Jean‐Christophe Mulatier Dr. Jean‐Pierre Dutasta Dr. Laure Guy Prof. Alexandre Martinez 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(6):2068-2074
A convenient and efficient gram‐scale synthesis for enantiopure hemicryptophane–tren (tren=tris(2‐aminoethyl)amine) derivatives has been developed. The four‐step synthesis is based on the optical resolution of a key intermediate, cyclotriveratrylene, for which the energy barrier for racemization has been measured to ensure that no racemization occurs during the two last steps of the synthetic pathway. The assignments of the absolute configurations have been performed by electronic circular dichroism and the enantiopurity was determined by NMR spectroscopy in the presence of enantiopure camphor sulfonic acid. To highlight the interest of such compounds, the recognition of norephedrine neurotransmitter was investigated and showed a remarkable enantioselectivity towards the C3 symmetrical hosts. Finally, this highly modular synthetic pathway was used to provide eight enantiopure hemicryptophanes with different sizes, shapes, and functionalities. These results underline the high potential of this approach, which could lead to many applications in chiral recognition or asymmetric supramolecular catalysis. 相似文献
36.
End group polarity and block symmetry effects on cloud point and hydrodynamic diameter of thermoresponsive block copolymers 下载免费PDF全文
Xu Xiang Xiaochu Ding Ning Chen Beilu Zhang Patricia A. Heiden 《Journal of polymer science. Part A, Polymer chemistry》2015,53(24):2838-2848
Thermoresponsive block copolymers are of interest for delivery vehicles in the body. Often an interior domain is designed for the active agent and the exterior domain provides stability in the bloodstream, and may carry a targeting ligand. There is still much to learn about how block sequence and chain end identity affect micelle structure, size, and cloud points. Here, hydrophilic oligo(ethylene glycol) methyl ether acrylate and more hydrophobic di(ethylene glycol) methyl ether methacrylate monomers were polymerized to give amphiphilic block copolymers with amphiphilic chain ends. The block sequence and chain end identity were both controlled by appropriate choice of RAFT chain transfer agents to study the effect of ‘matched’ and ‘mismatched’ chain end polarity with amphiphilic block sequence. The affect of matching or mismatching chain end polarity and block sequence was studied on the hydrodynamic diameter, cloud point, and temperature range of the chain collapse on linear di‐ and triblock copolymers and star diblock polymers. The affects of matching or mismatching chain end polarity were significant with linear diblock copolymers but more complex with triblock and star copolymers. Explanations of these results may help guide others in designing thermoresponsive block copolymers. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 2838–2848 相似文献
37.
Specificity of Furanoside–Protein Recognition through Antibody Engineering and Molecular Modeling 下载免费PDF全文
Dr. Parnian Lak Spandana Makeneni Prof. Dr. Robert J. Woods Prof. Dr. Todd L. Lowary 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(3):1138-1148
Recognition of furanosides (five‐membered ring sugars) by proteins plays important roles in host–pathogen interactions. In comparison to their six‐membered ring counterparts (pyranosides), detailed studies of the molecular motifs involved in the recognition of furanosides by proteins are scarce. Here the first in‐depth molecular characterization of a furanoside–protein interaction system, between an antibody (CS‐35) and cell wall polysaccharides of mycobacteria, including the organism responsible for tuberculosis is reported. The approach was centered on the generation of the single chain variable fragment of CS‐35 and a rational library of its mutants. Investigating the interaction from various aspects revealed the structural motifs that govern the interaction, as well as the relative contribution of molecular forces involved in the recognition. The specificity of the recognition was shown to originate mainly from multiple CH–π interactions and, to a lesser degree, hydrogen bonds formed in critical distances and geometries. 相似文献
38.
Generic applications of 13C‐detected NMR diffusion to formulated systems with suppression of thermal convection induced by proton decoupling 下载免费PDF全文
Jianbo Hou Yiyong He Paolo Sabatino Ling Yuan David Redwine 《Magnetic resonance in chemistry : MRC》2016,54(7):584-591
Fast and effective structural/compositional analysis on formulated systems represents one of the major challenges encountered in analytical science. 13C‐detected diffusion represents a promising tool to tackle the aforementioned challenges, particularly in industry. Toward exploring the generic applications of 13C‐detected diffusion, thermal convection induced by 1H decoupling has been identified as a key factor that resulted in significantly reduced resolution in the diffusion dimension. Optimization of experimental parameters and utilization of double‐stimulated echo‐based pulse sequence both can effectively suppress the thermal convection caused by the 1H decoupling, the success of which allows robust and generic applications of 13C‐detected diffusion to systems from mixtures of small molecules, polymer blends, and copolymers to actual complex formulated systems. The method is particularly powerful in differentiating small molecules from polymers, polymer blends from copolymers, and end‐group analysis. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
39.
Thioetherphenolate group 4 metal complexes in the ring opening polymerization of rac‐β‐Butyrolactone 下载免费PDF全文
Ermanno Luciano Antonio Buonerba Alfonso Grassi Stefano Milione Carmine Capacchione 《Journal of polymer science. Part A, Polymer chemistry》2016,54(19):3132-3139
Group 4 complexes 1 – 3 [ 1 = (t‐BuOS)2Ti(O‐i‐Pr)2; 2 = (t‐BuOS)2Zr(O‐t‐Bu)2; 3 = (t‐BuOS)2Hf(O‐t‐Bu)2] supported by two phenolate bidentate ligands (t‐BuOS‐H = 4,6‐di‐tert‐butyl‐2‐phenylsulfanylphenol) promote the well‐controlled ring opening polymerization of rac‐β‐butyrolactone. In presence of isopropanol, low dispersities and molecular weights proportional to the equivalents of isopropanol are achieved. Moreover, the zirconium complex is effective in the copolymerization of rac‐β‐butyrolactone with rac‐lactide. The 13 C nuclear magnetic resonance analysis revealed that the obtained copolymers have a tapered diblock microstructure consisting of an initial block composed of lactide sequences and a terminal block composed of butyrolactone sequences. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 3132–3139 相似文献
40.
Dominik Vítek Prof. Aleš Růžička Lise Vermeersch Dr. Libor Dostál Dr. Jan Turek Prof. Roman Jambor 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(70):e202202639
Reactivity studies of the GeII→B complex L(Cl)Ge⋅BH3 ( 1 ; L=2-Et2NCH2-4,6-tBu2-C6H2) were performed to determine the effect on the GeII→B donation. N-coordinated compounds L(OtBu)Ge⋅BH3 ( 2 ) and [LGe⋅BH3]2 ( 3 ) were prepared. The possible tuning of the GeII→B interaction was proved experimentally, yielding compounds 1-PPh2-8-(LGe)-C10H6 ( 4 ) and L(Cl)Ge⋅GaCl3 ( 5 ) without a GeII→B interaction. In 5 , an unprecedented GeII→Ga coordination was revealed. The experimental results were complemented by a theoretical study focusing on the bonding in 1 − 5 . The different strength of the GeII→E (E=B, Ga) donation was evaluated by using energy decomposition analysis. The basicity of different L(X)Ge groups through proton affinity is also assessed. 相似文献