• 제목/요약/키워드: exchange ring

검색결과 106건 처리시간 0.021초

An Ethernet Ring Protection Method to Minimize Transient Traffic by Selective FDB Advertisement

  • Lee, Kwang-Koog;Ryoo, Jeong-Dong;Min, Seung-Wook
    • ETRI Journal
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    • 제31권5호
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    • pp.631-633
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    • 2009
  • We introduce an improved Ethernet ring protection method, selective filtering database (FDB) advertisement, to minimize traffic overshoot in the event of a failure or recovery. On the protection switching event, the proposed method makes all ring nodes perform an FDB flush except the FDB entries associated with their client subnets. Then, ring nodes rapidly exchange their client MAC address lists so that their FDBs are immediately updated by indirect MAC address learning. The proposed scheme guarantees fast and reliable protection switching over the standard scheme.

ON A GENERALIZATION OF UNIT REGULAR RINGS

  • Tahire Ozen
    • 대한수학회보
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    • 제60권6호
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    • pp.1463-1475
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    • 2023
  • In this paper, we introduce a class of rings generalizing unit regular rings and being a subclass of semipotent rings, which is called idempotent unit regular. We call a ring R an idempotent unit regular ring if for all r ∈ R - J(R), there exist a non-zero idempotent e and a unit element u in R such that er = eu, where this condition is left and right symmetric. Thus, we have also that there exist a non-zero idempotent e and a unit u such that ere = eue for all r ∈ R - J(R). Various basic characterizations and properties of this class of rings are proved and it is given the relationships between this class of rings and some well-known classes of rings such as semiperfect, clean, exchange and semipotent. Moreover, we obtain some results about when the endomorphism ring of a module in a class of left R-modules X is idempotent unit regular.

Generic Constructions for Strong Designated Verifier Signature

  • Feng, Deng-Guo;Xu, Jing;Chen, Wei-Dong
    • Journal of Information Processing Systems
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    • 제7권1호
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    • pp.159-172
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    • 2011
  • A designated verifier signature is a special type of digital signature, which convinces a designated verifier that she has signed a message in such a way that the designated verifier cannot transfer the signature to a third party. A strong designated verifier signature scheme enhances the privacy of the signer such that no one but the designated verifier can verify the signer's signatures. In this paper we present two generic frame works for constructing strong designated verifier signature schemes from any secure ring signature scheme and any deniable one-pass authenticated key exchange protocol, respectively. Compared with similar protocols, the instantiations of our construction achieve improved efficiency.

Radical Ring-Crossover Polymerization of Macrocycles with Radically Exchangeable Dynamic Covalent Bonds

  • Otsuka, Hideyuki;Yamaguchi, Go;Takahara, Atsushi
    • 한국고분자학회:학술대회논문집
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    • 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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    • pp.320-320
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    • 2006
  • The authors report the synthesis and radical ring-crossover polymerization of macrocycles with radically exchangeable dynamic covalent bonds. The macrocyclic compounds with alkoxyamine units were designed and synthesized by condensation from alkoxyamine-based diol and the corresponding acid chlorides in the presence of pyridine under high-dilution condition. The macrocycles can thermally polymerize by intermolecular radical crossover reaction. Furthermore, the poly(alkoxyamine)s depolymerized to the monomers principally by the intramolecular radical exchange process under high-dilution conditions.

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Polymer-Supported Crown Ethers(Ⅳ) Synthesis and Phase-transfer Catalytic Activity

  • Shim Jae Hu;Chung Kwang Bo;Masao Tomoi
    • Bulletin of the Korean Chemical Society
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    • 제13권3호
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    • pp.274-279
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    • 1992
  • Immobilization method of lariat azacrown ethers, containing hydroxyl group in the side arm of crown ring, on the polymer matrix and the phase-transfer catalytic activity of thus obtained immobilized lariat azacrown ethers were studied. Polystyrene resins with crown ether structures and hydroxyl groups adjacent to the macrorings were prepared by the reaction of crosslinked polystyrene resins containing epoxy groups with monoaza-15-crown-5 or monoaza-18-crown-6. Microporous crosslinked polystyrene resins containing epoxy group for the syntheses of these immobilized lariat crown catalysts were prepared by suspension polymerization of styrene, divinylbenzene (DVB 2%) and vinylbenzylglycidyl ether. The immobilized lariat catalysts with 10-20% ring substitution exhibited maximal activity for the halogen exchange reactions of 1-bromooctane with aqueous KI or NaI under triphase heterogeneous conditions. Immobilized catalyst exhibited higher activity than corresponding catalyst without the hydroxyl group and this result was suggested that the active site have a structure in which the $K^+$ ion was bound by the cooperative coordination of the crown ring donors and the hydroxyl group in the side arm.

An NMR Study on Complexation of Cesium Ion by p-tert-Butylcalix[6]arene Ethyl Ester

  • Chung, Kee-Choo;Namgoong, Hyun;Lee, Jo-Woong
    • Bulletin of the Korean Chemical Society
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    • 제25권5호
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    • pp.609-616
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    • 2004
  • Complexation of cesium ion by p-tert-butylcalix[6]arene ethyl ester was studied by NMR spectroscopy in nonpolar $CDCl_3$ and polar acetone-$d_6$ and the results were compared with each other. Analysis of temperature dependent $^1H$ spectra and titration curves reveals that both solvents result in a 1 : 1 cone-form complex with nonpolar $CDCl_3$yielding a more tightly bound one than acetone-$d_6$. Unexpectedly, at very low temperature, we have found that two phenyl ring proton peaks of equal intensity appear both in $CDCl_3$and in acetone-$d_6$ solution which gradually collapse and eventually coalesce into a single line as temperature is raised. This observation could be interpreted in terms of the chemical exchange through direct and/or indirect interconversion between two equivalent conformations possible the complex in both solvents over the temperature range observed. And broadening of $^{133}Cs$ (I = 7/2) nmr line with increasing temperature has also been observed, indicating the exchange of $^{133}Cs$ ion between the complex and the solvent. From numerical fitting of lineshape changes for one-dimensional $^1H$ and $^{133}Cs$ spectra, the exchange rate constants and other relevant parameters for this conformational interconversion and the complex-solvent exchange were deduced.

유비쿼터스 전자거래를 위한 쓰레시홀드 링 그룹 서명 (A Threshold Ring Group Signature for Ubiquitous Electronic Commerce)

  • 성순화
    • 정보처리학회논문지D
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    • 제14D권4호
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    • pp.373-380
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    • 2007
  • 유비쿼터스 전자거래를 통하여 사용자는 언제 어디서나 네트워크에 접근하여 편리한 정보를 개인과 그룹, 그룹과 그룹 사이에서 교환할 수 있다. 사용자가 이러한 유비쿼터스 전자거래를 안전하게 사용하기 위해서는, 전자 정보의 무결성과 인증의 특성을 가지는 디지털 서명이 필수 조건이다. 유비쿼터스 네트워크에서의 디지털 서명은 언제 어디서나 필요에 따라 그룹을 만들기도 하고 해체하기도 하므로, 유비쿼터스 전자거래는 신뢰된 그룹 관리자와 셋업 프로시져 철회 프로시져 등이 필요 없는 디지털 서명이 요구된다. 따라서 본 논문에서는 안전한 유비쿼터스 전자거래를 위한 디지털 서명으로서 쓰레시홀드 링 서명을 제안한다. 제안된 디지털 서명은 위조의 위험이 없는(무결성) 링 서명과 메시지가 다른 서명자에 의해 서명되는 것을 증명할 수 없는 문제를 해결하는(인증) (n,t)링 서명을 사용한다. 그러므로 제안된 쓰레시홀드 링 서명은 무결성과 인증을 만족하는 차세대 유비쿼터스 그룹 서명이다.

Rates of Conformational Change of 3,3-Dimethylpiperidine and Solvent Effects on Its Conformation When Coordinated to the Paramagnetic Undecatungstocobalto(II)silicate Anion Studied by 1H NMR Spectroscopy

  • 현재원;소현수
    • Bulletin of the Korean Chemical Society
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    • 제18권9호
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    • pp.961-965
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    • 1997
  • 1H NMR spectra of 3,3-dimethylpiperidine (1) at -70 to 30 ℃ exhibit gradual change from slow to rapid exchange between two alternate chair forms. The exchange rate constant was determined as a function of temperature by simulating the line shape of the signal from the two methyl groups using the modified Bloch equations. The resulting free energy of activation is ΔG* = 44.4±1.9 kJ mol-1 at 298 K. The 1H NMR spectrum of a D2O or dimethylsulfoxide-d6 (DMSO-d6) solution containing 1 and [SiW11CoⅡO39]6- exhibits separate signals for the free ligand and the complex, indicating that the ligand exchange is slow on the NMR time scale. In D2O the piperidine ring is frozen as a chair form even at room temperature with the cobalt ion bonded to the axial position of the nitrogen atom. When DMSO-d6 is added to the D2O solution, the NMR spectral change suggests that a rapid exchange occurs between the chair form and another conformer. It is proposed that the conformation of ^b1^b coordinated to [SiW11CoⅡO39]6- in DMSO-d6 is close to a twist form.

A STATISTICAL STUDY OF MAGNETIC STORM RECOVERY PHASE: PRELIMINARY RESULTS

  • Lee, D.Y.;Hwang, J.A.;Min, K.W.;Lee, E.S.;Cho, K.S.;Kim, S.G.;Bae, S.H.
    • Journal of Astronomy and Space Sciences
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    • 제18권1호
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    • pp.27-32
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    • 2001
  • A statistical study has been performed of the magnetic storm recovery phase using the Dst index for 102 storm events in the interval January 1996 to December 1998. In 43 cases (or 42%) out of our 102 events, the recovery phase exhibits fast recovery (kaking about 8 hours or less) at its initial stage or for the entire recovery period. Since this fast recovery can be explained by the fast charge exchange less of $O^{+}$ ions which mostly com from the ionosphere, and since a fraction of $H^{+}$ ions is of ionospheric origin as well, our statistical result supports the view that the source of ring current ions in many magnetic storms can be terrestrial.

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