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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.

Structure Based Protein Engineering of Aldehyde Dehydrogenase from Azospirillum brasilense to Enhance Enzyme Activity against Unnatural 3-Hydroxypropionaldehyde

  • Son, Hyeoncheol Francis;Kim, Kyung-Jin
    • Journal of Microbiology and Biotechnology
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    • 제32권2호
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    • pp.170-175
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    • 2022
  • 3-Hydroxypropionic acid (3HP) is a platform chemical and can be converted into other valuable C3-based chemicals. Because a large amount of glycerol is produced as a by-product in the biodiesel industry, glycerol is an attractive carbon source in the biological production of 3HP. Although eight 3HP-producing aldehyde dehydrogenases (ALDHs) have been reported so far, the low conversion rate from 3-hydroxypropionaldehyde (3HPA) to 3HP using these enzymes is still a bottleneck for the production of 3HP. In this study, we elucidated the substrate binding modes of the eight 3HP-producing ALDHs through bioinformatic and structural analysis of these enzymes and selected protein engineering targets for developing enzymes with enhanced enzymatic activity against 3HPA. Among ten AbKGSADH variants we tested, three variants with replacement at the Arg281 site of AbKGSADH showed enhanced enzymatic activities. In particular, the AbKGSADHR281Y variant exhibited improved catalytic efficiency by 2.5-fold compared with the wild type.

1,5,3,7-Diazadiphosphocine-1,5-Dicarboxylic Acids의 합성과 반응 (Synthesis and Reaction of 1,5,3,7-Diazadiphosphocine-1,5-Dicarboxylic Acids)

  • 조승환;송주현;이도훈;이용균;박유미;최순규;한정태;정대일
    • 생명과학회지
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    • 제17권7호통권87호
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    • pp.910-914
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    • 2007
  • 본 연구는 MRI 조영제나 새로운 생리활성 물질을 개발키 위해 paraformaldehyde와 hypophosphorous acid를 아미노산인 glycine 혹은 glutamic acid와 함께 반응시켜 3,7-dihydroxy-3,7-dioxoperhydro-1,5,3,7-diazadiphos-phocme-1,5-diacetic acid 1 와 3,7-dihydrexy-3,7-dioxoperhydre-1,5,3,7-diazadiphos-phocme-1,5-di- (2-glutaric acid)3을 합성하였다. 그러나 aspartic acid에 의한 2-[5-(1,2-dicarboxy-ethyl)-3,7-dihydroxy-3,7-dioxo-315.715-[1,5,3,7]diazadiphosphocan-1-yl]-succinic acid 2는 얻지 못했다. 합성 된 3,7-dihydroxy-3,7-dioxoperhydro-1,5,3,7-dia-zadiphosphocine-1,5-diacetic acid 1을 산 촉매에 의한 에스테르화반응시켜 화합물 3,7-dihydroxy-3,7-dioxoper-hydro-1,5,3,7-diazadiphosphocine-1,5-diacetic acid methyl ester 4, 3,7-dihydroxy-3,7-dioxoperhydro-1,5,3,7-dia-zadiphosphocine-1,5-diacetic acid ethyl ester 5, 그리고 3,7-dihyoxy-3,74dioxoperhyo-1,5,3,7-diazadiphosphocine-1,5-diacetic acid propyl ester 6을 합성하였다. 계속해서 다양한 반응을 통해 새로운 화합물을 합성할 것이며 생리활성검색도 실시할 예정이다.

LiNi1/3Mn1/3Co1/3O2계 정극활물질을 적용한 전극 제조조건 최적화 연구 (A Study on Optimization of Manufacturing Condition for LiNi1/3Mn1/3Co1/3O2-based Cathode Electrode)

  • 김현수;김성일;이창우;문성인;김우성
    • 한국전기전자재료학회논문지
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    • 제19권2호
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    • pp.139-144
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    • 2006
  • A fabrication condition of the cathode electrode was optimized in a lithium secondary battery. The $LiNi_{1/3}Mn_{1/3}Co_{1/3}O_2$ powders were used as a cathode material. The $LiNi_{1/3}Mn_{1/3}Co_{1/3}O_2$/Li cells were prepared with a certain formulation and their cycleability and rate-capability were evaluated. Optimum electrode composition simulated from the evaluated value was 86.3: 5.6: 8.1 in mass $\%$ of active material: binder: conducting material. Discharge capacity decreased markedly as the press ratio exceeded $30\%$ during preparation of the electrode. Discharge performance at a high current rate deteriorated abruptly as the electrode thickness was over $120{\mu}m$.

3-D CT Imaging of Pathological Bone Changes in a Rat Model of Adjuvant-Induced Arthritis

  • Shim, Kyung-Mi;Kim, Se-Eun;Kang, Seong-Soo
    • 한국방사선학회논문지
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    • 제2권4호
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    • pp.41-46
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    • 2008
  • CT는 단층촬영을 이용한 의학적인 영상 진단 기법이다. CT는 3차원적인 방사선학적 영상 기법으로 염증의 평가에는 적합하지 않으나, 석회화된 조직을 직접적인 3차원 영상으로 보여주므로 뼈 손상의 평가에는 유용하다. 본 연구는 실험적으로 유도된 랫드의 보조관절염에서 관절의 병리학적 변화와 뼈 파괴의 정량적 분석을 3차원 CT 영상을 통하여 평가하고자 실시되었다. 그 결과 랫드의 보조관절염에서 병변의 파괴성 진행이 3차원 CT 영상을 통해 정량화될 수 있었고, 따라서 관절염 질환의 상태 및 실험적인 치료 약제의 효능 평가에 3차원 CT 영상 기법이 효과적일 것으로 생각된다.

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인체 모델 생성을 위한 등고선 삼각분할 기반의 3차원 전신 스캐너 개발 (Development of a 3D Whole Body Scanner for Reconstructing Human Body based on Contour Triangulation Technique)

  • 최영규;구본기;최병태
    • 한국정보과학회논문지:시스템및이론
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    • 제30권7_8호
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    • pp.397-407
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    • 2003
  • 인간의 신체에 대한 정확한 3차원 표면모델을 추출할 수 있는 기술에 대한 요구와 관심이 최근 멀티미디어 등 다양한 응용 분야에서 증폭되고 있다. 본 논문에서는 인체의 ,3차원 모델을 효율적으로 추출하기 위한, 3차원 스캐너를 소개하였으며, 취득된 3차원 정보로부터 등고선(Wire-frame Contour)을 안정적으로 생성하는 반자동 등고선 생성 방법을 제안하였다. 또한 생성된 등고선으로부터 3차원 표면모델을 추출하기 위한 표면 삼각분할 알고리즘을 제안하였다. 실험을 통해 개발된 시스템과 제안된 방법이 안정적이고 효과적으로 인체의, 3차원 표면모델을 생성하는 것을 확인할 수 있었다.

Synthesis and Molecular Structure of p-tert-butylcalix[4]arene Hexanoate

  • Park, Young-Ja;Kwanghyun No;Cho, Sun-Hee
    • 한국결정학회지
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    • 제10권1호
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    • pp.1-8
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    • 1999
  • Two conformational isomers of p-tert-butylcalix[4]arene hexanoate were prepared from the reaction of-p-tert-butylcalix[4]arene and hexanoly chloride in the presence of AlCl3 in CH2Cl2 and their structures were determined by NMR spectra and X-ray diffraction as a cone and a 1,3-alternate conformer, respectively. The crystal of cone conformer (C68H96O8·(CH3)2CO) is triclinic, P, a=15.066(1) , b=16.063(1) , c=16.365(1) , α=79.75(2)o, β=109.95(2)o, γ=80.32(0)o, V=3602.7(4) 3, Z=2. The intensity data were collected on Simens SMART diffractometer/CCD area detector. The structure was solved by direct method and refined by least-squares calculations to a final R value of 0.144 for 4638 observed reflections. The molecular conformation is distorted symmetric cone with the flattening A and D phenyl rings. The crystal of 1,3-alternate conformer (C68H96O8·2CHCl3) is orthorhombic, Pca21, a=34.586(5) , b=10.207(3) , c=20.394(4) , V=7199(3) 3, Z=4. The intensity data were collected on an Enraf-Noninus CAD-4 Diffractometer with a graphite monochromated Mo-K radiation. The structure was solved by direct method and refined by least-squares calculations to a final R value of 0.152 for 2241 observed reflections. The molecule has a pseudo mirror symmetric 1,3-alternate conformation.

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Accuracy evaluation of dental models manufactured by CAD/CAM milling method and 3D printing method

  • Jeong, Yoo-Geum;Lee, Wan-Sun;Lee, Kyu-Bok
    • The Journal of Advanced Prosthodontics
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    • 제10권3호
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    • pp.245-251
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    • 2018
  • PURPOSE. To evaluate the accuracy of a model made using the computer-aided design/computer-aided manufacture (CAD/CAM) milling method and 3D printing method and to confirm its applicability as a work model for dental prosthesis production. MATERIALS AND METHODS. First, a natural tooth model (ANA-4, Frasaco, Germany) was scanned using an oral scanner. The obtained scan data were then used as a CAD reference model (CRM), to produce a total of 10 models each, either using the milling method or the 3D printing method. The 20 models were then scanned using a desktop scanner and the CAD test model was formed. The accuracy of the two groups was compared using dedicated software to calculate the root mean square (RMS) value after superimposing CRM and CAD test model (CTM). RESULTS. The RMS value ($152{\pm}52{\mu}m$) of the model manufactured by the milling method was significantly higher than the RMS value ($52{\pm}9{\mu}m$) of the model produced by the 3D printing method. CONCLUSION. The accuracy of the 3D printing method is superior to that of the milling method, but at present, both methods are limited in their application as a work model for prosthesis manufacture.

가구디자인에서 3D Printer의 활용 현황에 관한 연구 (A Study on the Status of the 3D Printer in Furniture Design)

  • 강현대
    • 한국가구학회지
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    • 제26권4호
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    • pp.383-391
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    • 2015
  • In recent years the industry has utilized some of the 3D printers in the manufacturing process a trend which spread also a personal desktop 3D printer priced. The 3D printer can create the 3D object by using an ink or a laser instead of the powders, and various liquid plastic material. Properties of 3D printers are liquid, solid, powder and raw materials are also classified as varied. New ideas and processes in the form of designer furniture, becoming increasingly evolved through the development of materials and technologies. Science, art and technology combine to create a new aesthetic for the complex and free binding structure is a combination of design and materials are available in craft and the structure appears not showing. 3D scanning was not simply continue to develop as the production process by a variety of tools and content transformation. Create new mathematical tables and chairs designed by the theory fit the digital age shows a coupling structure with decoration into small pieces. It has created a new craft technique in the digital age.

H2S 제거를 위한 Zeolite와 DETOX의 흡착 특성 비교 연구 (A Study on the comparison on Adsorption characteristics of Zeolite and DETOX for the removal of H2S)

  • 박대석;임지영;조영근;송승준;김진한
    • 한국산학기술학회논문지
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    • 제15권7호
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    • pp.4675-4681
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    • 2014
  • 본 연구는 흡착제 Zeolite 3A와 DETOX에 대하여 $H_2S$의 유입농도와 흡착온도를 공정변수로 하여 포화시간, 흡착량, 흡착속도 등의 $H_2S$ 흡착 제거특성을 평가하기 위하여 수행되었다. $H_2S$의 유입질량유속이 증가함에 따라 Zeolite 3A의 흡착용량은 증가되었으나 포화시간은 감소되었다. 한편 DETOX의 흡착용량과 포화시간은 $H_2S$의 유입질량유속의 증가에 따라 감소되었다. 흡착온도가 상승함에 따라 Zeolite 3A의 흡착용량과 포화시간은 감소한 반면에, DETOX에 대한 이들 값은 증가하였다. DETOX의 $H_2S$흡착용량은 Zeolite 3A의 2.5~16.4배 정도 높게 나타났다. 이는 흡착에서 활성화에너지장벽을 넘어설 충돌빈도는 흡착온도가 증가함에 따라 증가한 것에 기인한 것으로 해석된다. Zeolite 3A와 DETOX에 대하여 $H_2S$의 흡착속도는 $H_2S$의 유입질량유속과 흡착온도가 증가함에 따라 증가하였다. $H_2S$의 흡착속도는 Zeolite 3A가 DETOX의 4배로 나타났다. DETOX는 Zeolite 3A에 비하여 온도 308~318K에서 포화시간은 더욱 길어지고 흡착용량은 더욱 커진다. 바이오가스 중의 $H_2S$제거에 있어서 DETOX는 Zeolite 3A에 비하여 유리한 것으로 나타났다.