• Title/Summary/Keyword: chain rings

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CYCLIC CODES OVER THE RING 𝔽p[u, v, w]/〈u2, v2, w2, uv - vu, vw - wv, uw - wu〉

  • Kewat, Pramod Kumar;Kushwaha, Sarika
    • Bulletin of the Korean Mathematical Society
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    • v.55 no.1
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    • pp.115-137
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    • 2018
  • Let $R_{u{^2},v^2,w^2,p}$ be a finite non chain ring ${\mathbb{F}}_p[u,v,w]{\langle}u^2,\;v^2,\;w^2,\;uv-vu,\;vw-wv,\;uw-wu{\rangle}$, where p is a prime number. This ring is a part of family of Frobenius rings. In this paper, we explore the structures of cyclic codes over the ring $R_{u{^2},v^2,w^2,p}$ of arbitrary length. We obtain a unique set of generators for these codes and also characterize free cyclic codes. We show that Gray images of cyclic codes are 8-quasicyclic binary linear codes of length 8n over ${\mathbb{F}}_p$. We also determine the rank and the Hamming distance for these codes. At last, we have given some examples.

N-Tosyl Calix[4]arene Azacrown Ether, $C_{45}H_{49}NO_6S$

  • Kim, Jong-Seung;Kim, Moon-Jib;Choo, Geum-Hong;Lee, Jin-Ho;Suh, Il-Hwan
    • Korean Journal of Crystallography
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    • v.10 no.1
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    • pp.66-70
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    • 1999
  • The calix[4]arene molecule adopting the 1,3-alternate conformation forms a square cavity, and two pair phenyl rings lying above and below a least-square plane defined by the four bridging methylene groups in the calix[4]arene are widened upwards and downwards, respectively, from central axis, which leads to O1-O4=4.064 and O2-O3=3.864 . Two propyloxy groups are stabilized with all trans conformations, but the rather short azacrown ether chain with two oxygen atoms includes cis/trans conformations with O1-C35=2.906 . Therefore the cavity does not seem to be big enough to form a host-guest complex.

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Synthesis, Cytotoxicity and Topoisomerase II Inhibitory Activity of Benzonaphthofurandiones

  • Rhee, Hee-Kyung;Kwon, Young-Joo;Chung, Hwa-Jin;Lee, Sang-Kook;ParkChoo, Hea-Young
    • Bulletin of the Korean Chemical Society
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    • v.32 no.7
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    • pp.2391-2396
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    • 2011
  • Benzonaphthofurandiones containing four coplanar fused aromatic rings were synthesized and evaluated for their cytotoxicity against five human cancer cell lines, and their inhibitory activity on topoisomerases. These benzonaphthofurandiones were prepared by condensation of 2,3-dichloronaphthoquinone and three aromatic diols with base catalysts in alcohol. The synthesized compounds were o-alkylated with six dialkylaminoalkyl halides. The hydroxy derivatives (8a-8g) exhibited relatively potent cytotoxicity among the prepared compounds. These compounds were evaluated as excellent inhibitors against topoisomerase II (topo II). Especially, the hydroxy analogue with branched methyl side chain (8e) showed high cytotoxicity against cancer cell lines and good inhibitory activity on topo II.

FINITELY t-VALUATIVE DOMAINS

  • Chang, Gyu Whan
    • Korean Journal of Mathematics
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    • v.22 no.4
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    • pp.591-598
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    • 2014
  • Let D be an integral domain with quotient field K. In [1], the authors called D a finitely valuative domain if, for each $0{\neq}u{\in}K$, there is a saturated chain of rings $D=D_0{\varsubsetneq}D_1{\varsubsetneq}{\cdots}{\subseteq}$ $D_n=D[x]$, where x = u or $u^{-1}$. They then studied some properties of finitely valuative domains. For example, they showed that the integral closure of a finitely valuative domain is a Pr$\ddot{u}$fer domain. In this paper, we introduce the notion of finitely t-valuative domains, which is the t-operation analog of finitely valuative domains, and we then generalize some properties of finitely valuative domains.

Synthesis, Protonation Constants and Stability Constants for Transition Metal ions(II) of 1, 15-Bis(2-Hydroxybenzyl)-2, 6, 10, 14-Tetraazapentadecane (1, 15-Bis(2-Hydroxybenzyl)-2, 6, 10, 14-Tetraazapentadecane 리간드합성, 양성자 해리상수 및 전이금속에 대한 안정도 상수결정)

  • Kim, Sun-Deuk;Kim, Jun-Kwang;Lee, Woo-Sik
    • Analytical Science and Technology
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    • v.13 no.6
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    • pp.810-814
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    • 2000
  • The open-chain hexadentate $N_4$, $O_2$ ligands 1, 15-bis(2-hydroxybenzyl)-2, 6, 10, 14-tetraazapentadecane (BSATPD. 4HCl) has been synthesized as its tetrahydro-chloride salt and characterized by EA, IR, NMR, and Mass spectrum. Its protonation constants ($logK_n{^H}$) and stability constants ($logK_{ML}$) for $Cu^{2+}$, $Ni^{2+}$, $Co^{2+}$ and $Zn^{2+}$ ions were determined in aqueous solution by potentiometry and compared with those of analogous $N_4$, $O_2$ ligands contain ethtylenic spacers or propylenic spacers, which make six-membered chelate rings between the aliphatic nitrogen atoms.

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Dispersion of Aqueous $Al_2O_3$Suspensions with Electrolytes; Influence of the Counter Ion

  • Cecile Pagnoux;Richard Laucournet;Thierry Chartier;Baumard, Jean-Francois
    • The Korean Journal of Ceramics
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    • v.6 no.3
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    • pp.280-285
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    • 2000
  • The electrolyte, $(HO)_2C_6H_2(SO_3Na)_2H_2O $(Tiron), disperses efficiently alumina powder in aqueous media and stable suspensions with 60 vol% solid loading can be prepared. The strong adsorption of this additive is mainly due to the ability of the molecule to form chelate rings with the particle surface but electrostatic interactions between the surface charge and the anionic dispersant strongly influence the amount of Tiron adsorbed. By using a cationic exchange route to substitute the counter ion which neutralizes the sulfonate groups, new molecules of dispersant have been prepared, either with mineral cations as $Li^+,\; Na+^,\; NH_4^\;+$, or with organic cations as counter ion but organic counter ions lead to less to less viscous suspensions than $Na^+$ in particular when the number of carbon atoms of the aliphatic chain increases from 1 to 3.

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The Crystal Structure of 1,3-Alternate 25,27-Bis(1-propyloxy)calix[4]arene crown-6, $C_{44}H_{54}O_8$ (1,3-Alternate 25,27-Bis(1-propyloxy)calix[4]arene crown-6, $C_{44}H_{54}O_8$의 결정구조)

  • 김종승;이원구;추건홍;이창희;이진호;김문집;김진구;서일환
    • Korean Journal of Crystallography
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    • v.10 no.2
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    • pp.130-135
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    • 1999
  • The title compound consisting of a calix[4]arene molecule with four phenyl rings bridged by four methylene groups and arranged alternately in anti-orientation fashion, two 25,27-bis(1-pro-pyloxy) groups attached on the two lower rims of calix[4]arene, and crown-6 chain attached on the other set of lower rims of calix[4]arene offers a big cavity inside a molecule which might possess a potential for forming host-guest complexes. The molecular packing is accomplished by van der Waals forces.

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Studies in Remote Functionalization (Ⅰ). Synthesis and Spectroscopic Studies of 3$\alpha$, 5$\alpha$-Cyclosteroidal Substrates

  • Lee, Eun;Park, Sang-Kyu;Lee, Hee-Yoon;Kim, Wan-Joo
    • Bulletin of the Korean Chemical Society
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    • v.2 no.3
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    • pp.105-112
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    • 1981
  • Various $3{\alpha}$, $5{\alpha}$-cyclocholestan-6${\beta}-yl$ ethers were synthesized from solvolysis reactions of cholesteryl tosylate. ${3\alpha}$, $5{\alpha}$-Cyclocholestan-6${\beta}-yl$ sulfides were the sole products when cholesteryl tosylate was solvolyzed in thiol solvents. Diol solvolysis products were derivatized to aromatic esters, and nuclear magnetic resonance spectroscopic method was used to show that aromatic rings can approach C-18 methyl group and the side chain.

ARCHIMEDEAN SKEW GENERALIZED POWER SERIES RINGS

  • Moussavi, Ahmad;Padashnik, Farzad;Paykan, Kamal
    • Communications of the Korean Mathematical Society
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    • v.34 no.2
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    • pp.361-374
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    • 2019
  • Let R be a ring, ($S,{\leq}$) a strictly ordered monoid, and ${\omega}:S{\rightarrow}End(R)$ a monoid homomorphism. In [18], Mazurek, and Ziembowski investigated when the skew generalized power series ring $R[[S,{\omega}]]$ is a domain satisfying the ascending chain condition on principal left (resp. right) ideals. Following [18], we obtain necessary and sufficient conditions on R, S and ${\omega}$ such that the skew generalized power series ring $R[[S,{\omega}]]$ is a right or left Archimedean domain. As particular cases of our general results we obtain new theorems on the ring of arithmetical functions and the ring of generalized power series. Our results extend and unify many existing results.

Changes in Cytosolic $Ca^{2+}$ but not in cGMP Contents May be more Important to Nitric Oxide-Mediated Relaxation in Depolarized Vascular Smooth Muscle

  • Lee, Hyun-Seok;Chang, Ki-Churl
    • The Korean Journal of Physiology and Pharmacology
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    • v.2 no.1
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    • pp.63-68
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    • 1998
  • Nitric oxide (NO)-mediated relaxation in vascular smooth muscle involves not only activation of guanylate cyclase but also hyperpolarization of the membrane. It has been shown that depolarization decreases the [$Ca^{2+}$] sensitivity of myosin light chain kinase in arterial smooth muscle, and nitric oxide (NO)-mediated relaxation was attenuated in this situation. However, why potassium inhibits or attenuates the action of EDRF/NO is not clear. Therefore, we investigated the magnitude of relaxation and cGMP contents using measures known to release NO, such as photorelaxation, photo activated NO-mediated relaxation, and NO-donor (SNP)-mediated relaxation in porcine coronary arterial rings in which contractile conditions were made by different degree of depolarization, i.e., contraction in response to U46619 or U46619 plus KCl. In all cases, the magnitude of relaxation was significantly greater (P<0.05) in U46619-contracted rings than in U46619+KCl-contracted ones. Although accumulation of cGMP was evident with three measures employed in the present study, no difference was found in cGMP contents between U46619 and U46619+KCl conditions, indicating that the diminished relaxation in KCl containing solution is cGMP-independent mechanism(s). To understand this further, cytosolic $Ca^{2+}$ changes due to NO were compared in rat thoracic aorta by exploiting photoactivated NO using streptozotocin (STZ) that was contracted with either NE or KCl. Fura-3 $[Ca]_{cyt}$ signal caused by NO was small and transient in high $K^+$-, but large and sustained in NE-contracted aorta. The inhibitory potency of STZ expressed in terms of $IC_{50}$ was 5.14 and 3.88 ${\mu}M$ in NE and in high $K^+$, respectively. These results suggest that modification of the cellular mobilization of $Ca^{2+}$ rather than cGMP levels may be an important mechanism for the NO-mediated relaxation when vascular membrane is depolarized, such as atherosclerosis and hypertension.

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