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Khan Najeeb Alam,Akbar Saeed,Qureshi Muhammad Ali,Hameed Tooba,Khan Nadeem Alam 한국물리학회 2021 THE JOURNAL OF THE KOREAN PHYSICAL SOCIETY Vol.78 No.2
In this work, we explore the superposition of two well-known chaotic oscillators, namely, the Duffing double-well and the forced van der Pol with the fractional order derivative. The proportional fractional derivative has been taken for numerical simulations and highly chaotic solution to improve some information of security systems has been found. The existence and the uniqueness of a super system are stated in the form of theorems using the Lipschitz condition locally. The qualitative properties of chaotic dynamics are described by mean of Lyapunov exponent (LE), eigenvalues, bifurcation and Poincaré maps. The analog circuit is also intended, with the help of different physical instruments, to validate the superposition of chaotic systems. The randomness level of a superposition chaotic system is tested via standard test suite, and the qualified set of a 32-bit array with high haphazardness is used for encryption as well as decryption. Furthermore, a security analysis is performed using different parameters, such as the uncertainty, similarity etc. The outcomes for the properties, time evolution, phase portrait, and oscilloscopic views are presented in tabulated and graphical forms.
Kumar, Shiv,Khan, S.A.,Alam, Ozair,Azim, Rizwan,Khurana, Atul,Shaquiquzzaman, M.,Siddiqui, Nadeem,Ahsan, Waquar Korean Chemical Society 2011 Bulletin of the Korean Chemical Society Vol.32 No.7
4-Chlorotetrazolo[1,5-a]quinoxaline (III) was synthesized by azide (2+3) cycloaddition of 2,3-dichloroquinoxaline (II). Compound (III) on further refluxing with hydrazine hydrate furnished 4-hydrazinotetrazolo[1,5-a]quinoxaline (IV). Further refluxing of (IV) with different aromatic aldehydes in methanol yielded corresponding Schiff's bases V(a-j). Various 4-aminotetrazolo[1,5-a]quinoxaline based azetidinones VII(a-j) were synthesized by stirring the compounds V(a-j), at low temperature, with equimolar mixture of chloroacetylchloride & triethylamine in dry benzene, while 4-aminotetrazolo[1,5-a]quinoxaline based thiazolidinones VIII(a-j) were synthesized by refluxing Schiff's bases V(a-j) with thioglycolic acid in oil-bath. The structures of all the compounds were confirmed on the basis of $^1H$-NMR & FT-IR spectral data. All the newly synthesized compounds were screened for in-vitro antimicrobial activity against E. coli, S. aureus, K. pneumoniae & P. aeruginosa & antifungal activity against C. albicans. Few of them have exhibited the promising activity.
Shiv Kumar,S. A. Khan,Ozair Alam,Rizwan Azim,Atul Khurana,M. Shaquiquzzaman,Nadeem Siddiqui,Waquar Ahsan 대한화학회 2011 Bulletin of the Korean Chemical Society Vol.32 No.7
4-Chlorotetrazolo[1,5-a]quinoxaline (III) was synthesized by azide (2+3) cycloaddition of 2,3-dichloroquinoxaline (II). Compound (III) on further refluxing with hydrazine hydrate furnished 4-hydrazinotetrazolo[1,5-a]quinoxaline (IV). Further refluxing of (IV) with different aromatic aldehydes in methanol yielded corresponding Schiff’s bases V(a-j). Various 4-aminotetrazolo[1,5-a]quinoxaline based azetidinones VII(a-j) were synthesized by stirring the compounds V(a-j), at low temperature, with equimolar mixture of chloroacetylchloride & triethylamine in dry benzene, while 4-aminotetrazolo[1,5-a]quinoxaline based thiazolidinones VIII(a-j) were synthesized by refluxing Schiff’s bases V(a-j) with thioglycolic acid in oil-bath. The structures of all the compounds were confirmed on the basis of ^1H-NMR & FT-IR spectral data. All the newly synthesized compounds were screened for in-vitro antimicrobial activity against E. coli, S. aureus, K. pneumoniae & P. aeruginosa & antifungal activity against C. albicans. Few of them have exhibited the promising activity.