• 제목/요약/키워드: R2R

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STABILITY OF MULTIPLICATIVE INVERSE FUNCTIONAL EQUATIONS IN THREE VARIABLES

  • Lee, Eun-Hwi
    • 호남수학학술지
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    • 제34권1호
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    • pp.45-54
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    • 2012
  • In this paper, we prove stabilities of multiplicative functional equations in three variables such as $r(\frac{x+y+z}{3})-r(x+y+z)$=$\frac{2r(\frac{x+y}{2})r(\frac{y+z}{2})r(\frac{z+x}{2})}{r(\frac{x+y}{2})r(\frac{y+z}{2})+r(\frac{y+z}{2})r(\frac{z+x}{2})+r(\frac{z+x}{2})r(\frac{x+y}{2})}$ and $r(\frac{x+y+z}{3})+r(x+y+z)$=$\frac{4r(\frac{x+y}{2})r(\frac{y+z}{2})r(\frac{z+x}{2})}{r(\frac{x+y}{2})r(\frac{y+z}{2})+r(\frac{y+z}{2})r(\frac{z+x}{2})+r(\frac{z+x}{2})r(\frac{x+y}{2})}$.

Relationship between Myosin Isoforms and Meat Quality Traits in Pig Semitendinosus Neuromuscular Compartments

  • Graziotti, Guillermo H.;Menendez, Jose M. Rodriguez;Rios, Clara M.;Cossu, Maria E.;Bosco, Alexis;Affricano, Nestor O.;Ceschel, Alejandra Paltenghi;Moisa, Sonia;Basso, Lorenzo
    • Asian-Australasian Journal of Animal Sciences
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    • 제24권1호
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    • pp.125-129
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    • 2011
  • The aim was to determine the relationship between muscle structure and meat quality traits in neuromuscular compartments (NMCs: R1, R2, R3, R4) of pig semitendinosus muscle. Barrows from the INTA-MGC genetic line (Argentina) were slaughtered at 100 kg body weight. In each NMC the following parameters were determined: the fibre types I, IIA, IIX and IIB by immunohistochemistry, the fibre cross sectional area (FCSA), the pH of meat after 24 h post-mortem ($pH_{24}$), instrumental meat tenderness (WB) and colour ($L^*$, $a^*$, $b^*$). There were significant differences in the following: $L^*$ (R1 = R4$a^*$ (R1>R4>R2 = R3), $b^*$ (R1 = R4R1 = R3 = R4), $pH_{24}$ (R1 = R4>R2 = R3). The relative percentages of FCSA were as follows: I (R4>R1>R3>R2), IIA (R1>R4>R3>R2), IIX (R1 = R2 = R3 = R4) and IIB (R2>R3>R1>R4). The correlation values were statistically significant between IIB and WB (R1 and R4, $r_s$ = 0.66), (R2 and R3 $r_s$ = 0.74), IIB and $L^*$ (R1 and R4 $r_s$ = 0.84), IIX and $L^*$ without discriminating NMCs. Our data suggest that the NMC where the sampling takes place is important for determining meat quality traits because of the heterogeneity of the whole muscle.

Syntheses and Structures of 1,2,3-Substituted Cyclopentadienyl Titanium(IV) Complexes

  • Joe, Dae-June;Lee, Bun-Yeoul;Shin, Dong-Mok
    • Bulletin of the Korean Chemical Society
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    • 제26권2호
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    • pp.233-237
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    • 2005
  • Cyclopentadiene compounds, 2-[CR'R(OMe)]-1,3-Me$_2C_5H_3$ (R, R' = 2,2'-biphenyl, 2) and 2-[CR'R(OSiMe$_3$)]-1,3-Me$_2C_5H_3$ (R, R' = 2,2'-biphenyl, 3; R = ph, R' = ph, 4; R = 2-naphthyl, R' = H, 5) are readily synthesized from 2-bromo-3-methoxy-1,3-dimethylcyclopentene (1). Reaction of the cyclopentadienes with Ti(NMe$_2$)$_4$ in toluene results in clean formation of the cyclopentadienyl tris(dimethylamido)titanium complexes, which are transformed to the trichloride complexes, 2-[CR'R(OMe)]-1,3-Me$_2C_5H_2$}TiCl$_3$ (R, R' = 2,2'-biphenyl, 6) and {2-[CR'R(OSiMe$_3$)]-1,3-Me$_2C_5H_2$}TiCl$_3$ (R, R' = 2,2'-biphenyl, 7; R = ph, R' = ph, 8; R = 2-naphthyl, R' = H, 9). Attempts to form C1-bridged Cp/oxido complexes by elimination of MeCl or Me$_3$SiCl were not successful. X-ray structures of 6, 7 and an intermediate complex {2-[Ph$_2$C(OSiMe$_3$)]-1,3-Me$_2C_5H_2$}TiCl$_2$(NMe$_2$) (10) were determined.

Stability of Low Temperature a-Si:H TFT on Stainless Steel Substrate

  • Kim, Sung-Hwan;Kim, Sang-Soo;Park, Yong-In;Peak, Seung-Han;Lee, Kyoung-Mook;Park, Choon-Ho;Lim, Yu-Sok;Kim, Chang-Dong;Kang, In-Byeong
    • 한국정보디스플레이학회:학술대회논문집
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    • 한국정보디스플레이학회 2008년도 International Meeting on Information Display
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    • pp.247-249
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    • 2008
  • Low Temperature a-Si:H TFT on stainless steel substrate has been developed for the flexible electrophoretic display. Stability of low temperature a-Si:H TFT is more important point than its initial device characteristics. Thus, we have studied device characteristics of low temperature a-Si:H TFT in terms of stability for driving electrophoretic display.

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Grignard Coupling Reaction of Bis(chloromethyl)diorganosilanes with Dichloro(diorgano)silanes: Syntheses of 1,3-Disilacyclobutanes

  • 조연석;유복렬;안삼영;정일남
    • Bulletin of the Korean Chemical Society
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    • 제20권4호
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    • pp.427-430
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    • 1999
  • The Grignard coupling reaction of bis(chloromethyl)diorganosilanes [(ClCH2)2SiR1R2: R1 = R2 = Me, la; R1 = Me, R2 = Ph, lb; R1 = R2 = Ph, lc] with diorganodichlorosilanes [(Cl2SiR3R4: R3 = R4 = Me, 2a; R3 = Me, R4 = Ph, 2b; R3 = R4 = Ph, 2c] at THE reflux temperature gave the intermolecular C-Si coupling product of 1,1,3,3-tetraorgano-1,3-disilacyclobutanes 3a-f in poor to moderate yields ranging from 7% to 50% along with polydiorganosilapropanes. The cyclization reaction of la-c with methyl-substituted dichlorosilanes 2a, b gave 1,3-disilacyclobutanes 3a-c, e, d in moderate yields (42-50%), while the same reaction with dichlorodiphenylsilane (2c) to 1,3-disilacyclobutanes 3d, f resulted in low yield (7-18%) probably due to the steric hindrance of two-phenyl groups on the silicon of 2c.

Two More Radicals for Right Near-Rings: The Right Jacobson Radicals of Type-1 and 2

  • Rao, Ravi Srinivasa;Prasad, K. Siva
    • Kyungpook Mathematical Journal
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    • 제46권4호
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    • pp.603-613
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    • 2006
  • Near-rings considered are right near-rings and R is a near-ring. $J_0^r(R)$, the right Jacobson radical of R of type-0, was introduced and studied by the present authors. In this paper $J_1^r(R)$ and $J_2^r(R)$, the right Jacobson radicals of R of type-1 and type-2 are introduced. It is proved that both $J_1^r$ and $J_2^r$ are radicals for near-rings and $J_0^r(R){\subseteq}J_1^r(R){\subseteq}J_2^r(R)$. Unlike the left Jacobson radical classes, the right Jacobson radical class of type-2 contains $M_0(G)$ for many of the finite groups G. Depending on the structure of G, $M_0(G)$ belongs to different right Jacobson radical classes of near-rings. Also unlike left Jacobson-type radicals, the constant part of R is contained in every right 1-modular (2-modular) right ideal of R. For any family of near-rings $R_i$, $i{\in}I$, $J_{\nu}^r({\oplus}_{i{\in}I}R_i)={\oplus}_{i{\in}I}J_{\nu}^r(R_i)$, ${\nu}{\in}\{1,2\}$. Moreover, under certain conditions, for an invariant subnear-ring S of a d.g. near-ring R it is shown that $J_2^r(S)=S{\cap}J_2^r(R)$.

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A NOTE ON THE MIXED VAN DER WAERDEN NUMBER

  • Sim, Kai An;Tan, Ta Sheng;Wong, Kok Bin
    • 대한수학회보
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    • 제58권6호
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    • pp.1341-1354
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    • 2021
  • Let r ≥ 2, and let ki ≥ 2 for 1 ≤ i ≤ r. Mixed van der Waerden's theorem states that there exists a least positive integer w = w(k1, k2, k3, …, kr; r) such that for any n ≥ w, every r-colouring of [1, n] admits a ki-term arithmetic progression with colour i for some i ∈ [1, r]. For k ≥ 3 and r ≥ 2, the mixed van der Waerden number w(k, 2, 2, …, 2; r) is denoted by w2(k; r). B. Landman and A. Robertson [9] showed that for k < r < $\frac{3}{2}$(k - 1) and r ≥ 2k + 2, the inequality w2(k; r) ≤ r(k - 1) holds. In this note, we establish some results on w2(k; r) for 2 ≤ r ≤ k.

trans-[Co(R,R-chxn)$_2Cl_2]^+$ 착물의 대이온 및 용매의존성 원편광이색성 스펙트라 (Circular Dichroism Spectra on the Counter Ions and the Solvent Dependence of trans-$[Co(R,R-chxn)_2Cl_2]^+$ Complex)

  • 오창언;김양;박성열;도명기
    • 대한화학회지
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    • 제35권5호
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    • pp.493-499
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    • 1991
  • 여러 가지 유기용매에서 서로 다른 대이온을 가진 trans-$[Co(R,R-chxn)_2Cl_2]^+$착물의 원편광이색성(CD) 스펙트럼을 측정하였다. 여기서 R,R-chxn은 (1R,2R)-1,2-diaminocyclohexane 이다. 착물의 CD 스펙트럼에서 관찰된 변화는 현저한 용매의존성을 나타내었다. 그리고 첫 흡수띠 영역$(^1A_{2g})$에서 CD 스펙트럼의 변화 정도는 용매의 donor number(DN)에 의존하였다. trans-[Co(R,R-chxn)$_2Cl_2]^+$ 착물의 CD 스펙트럼 변화는 $^1H$ NMR 스펙트럼으로부터 R,R-chxn 리간드 중의 수평방향의 N-H 수소와 용매분자와의 우선적인 상호작용에 기인되는 것으로 해석되었다.

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AN EXTREMAL PROBLEM ON POTENTIALLY $K_{r,r}$-ke-GRAPHIC SEQUENCES

  • Chen, Gang;Yin, Jian-Hua
    • Journal of applied mathematics & informatics
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    • 제27권1_2호
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    • pp.49-58
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    • 2009
  • For $1{\leq}k{\leq}r$, let ${\sigma}$($K_{r,r}$ - ke, n) be the smallest even integer such that every n-term graphic sequence ${\pi}$ = ($d_1$, $d_2$, ..., $d_n$) with term sum ${\sigma}({\pi})$ = $d_1$ + $d_2$ + ${\cdots}$ + $d_n\;{\geq}\;{\sigma}$($K_{r,r}$ - ke, n) has a realization G containing $K_{r,r}$ - ke as a subgraph, where $K_{r,r}$ - ke is the graph obtained from the $r\;{\times}\;r$ complete bipartite graph $K_{r,r}$ by deleting k edges which form a matching. In this paper, we determine ${\sigma}$($K_{r,r}$ - ke, n) for even $r\;({\geq}4)$ and $n{\geq}7r^2+{\frac{1}{2}}r-22$ and for odd r (${\geq}5$) and $n{\geq}7r^2+9r-26$.

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THE STRUCTURE OF SEMIPERFECT RINGS

  • Han, Jun-Cheol
    • 대한수학회지
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    • 제45권2호
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    • pp.425-433
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    • 2008
  • Let R be a ring with identity $1_R$ and let U(R) denote the group of all units of R. A ring R is called locally finite if every finite subset in it generates a finite semi group multiplicatively. In this paper, some results are obtained as follows: (1) for any semilocal (hence semiperfect) ring R, U(R) is a finite (resp. locally finite) group if and only if R is a finite (resp. locally finite) ring; U(R) is a locally finite group if and only if U$(M_n(R))$ is a locally finite group where $M_n(R)$ is the full matrix ring of $n{\times}n$ matrices over R for any positive integer n; in addition, if $2=1_R+1_R$ is a unit in R, then U(R) is an abelian group if and only if R is a commutative ring; (2) for any semiperfect ring R, if E(R), the set of all idempotents in R, is commuting, then $R/J\cong\oplus_{i=1}^mD_i$ where each $D_i$ is a division ring for some positive integer m and |E(R)|=$2^m$; in addition, if 2=$1_R+1_R$ is a unit in R, then every idempotent is central.