• Restorative Dentistry and Endodontics
• /
• v.34 no.1
• /
• pp.30-37
• /
• 2009

The purpose of this study was to evaluate the effect of pre-heating on some physical properties of composite resin. Eighty extracted, noncarious human molars were used in the present study. Four different temperatures of composite resin were used: $4^{\circ}C$, $17^{\circ}C$, $48^{\circ}C$, and $56^{\circ}C$. The $4^{\circ}C$ and $17^{\circ}C$ values represented the refrigerator storage temperature and room temperature respectively. For $48^{\circ}C$ and $56^{\circ}C$, composite resin was heated to the temperatures. As physical properties of composite resin, shear bond strength, microhardness, and degree of conversion were measured. The data for each group were subjected to one-way ANOVAs followed by the Tukey's HSD test at 95% confidence level. Both in enamel and dentin, among composite resin of $4^{\circ}C$, $17^{\circ}C$ $;48^{\circ}C$, and $56^{\circ}C$, the pre-heated composite resin up to $56^{\circ}C$ revealed the highest shear bond strength, and pre-heated composite resin to the higher temperature revealed higher shear bond strength. Microhardness value was also higher with composite resin of higher temperature. Degree of conversion was also higher with composite resin of the higher temperature. In this study, it seems that pre-heating composite resin up to the higher temperature may show higher shear bond strength, higher microhardness value, and higher degree of conversion. Therefore, when using composite resin in the clinic, preheating the composite resin could be recommended to have enhanced physical properties of it.

• Journal of the Korean Chemical Society
• /
• v.38 no.6
• /
• pp.405-410
• /
• 1994

Molecular orbital calculations suggest that an interaction between the psoralen derivatives of excite state and the thymine of ground state is dicussed in terms of their differing abilities to molecular complex. PM3-CI-UHF indicates that photocycloadducts across the C3-C4 and C4'-C5' double bonds of the methylpsoralen and hydroxypsoralen with thymine C5-C6 double bonds were deduced to be formed by their preferable frontier orbital interactions. The electronic properties of psoralen derivatives in the ground and excited states correlate with this difference in structure-activity relationship.

• Polymer(Korea)
• /
• v.24 no.6
• /
• pp.751-756
• /
• 2000

The copolymerization of ethylene (E) and cycloolefin (CO) was carried out with rac-Et(Ind)$_2$ZrC $l_2$ and MMAO cocatalyst system to examine the effect of CO structure on catalytic behaviors and properties of copolymer (COC). Various cycloolefins such as norbornene (N), 5-phenyl-2-norbornene (PN) and 5-vinyl-2-norbornene (VN) were used as comonomers. With increasing [CO]/[E] feed ratio, the catalytic activity decreased while the glass transition temperature of copolymer increased. With analysis of the structure of E/VN copolymer by FT-IR and $^{l3}$C-NMR, it was found that the cyclic C=C bond of VN comonomer is selectively polymerized and the vinyl C=C bond remains unreacted. The resulting vinyl C=C bond attached into copolymer provided the functionalization moiety using glycidyl methacrylate.e.

• Elastomers and Composites
• /
• v.43 no.4
• /
• pp.281-287
• /
• 2008

Using solid state $^{13}C$ NMR, polybutadiene rubber vulcanizates were qualitatively and quantitatively analyzed. In the filled conventional system of BR vulcanizate accelerated with TBBS, addition to the olefinic double bond and substitution in the $\alpha$ position to the double bond occurred simultaneously. Also the latter $\alpha$ substitution reaction was faster than the former addition reaction at initial reaction time. In addition, it was suggested that double bond-addition-polysulfide structures might be modified into 5-membered and 6-membered cyclic structures in overcure time. These chain modifications were correlated with the decrease in the chemical crosslink density in overcure time.

• Korean Journal of Food Science and Technology
• /
• v.28 no.3
• /
• pp.446-450
• /
• 1996

To investigate the effect of heating conditions on the polymerization of methyl linoleate, the esters were heated at $60^{\circ}C,\;90^{\circ}C,\;120^{\circ}C$ and $150^{\circ}C$, respectively, with sparging oxygen for different periods of time. On the basis of the peroxide curve obtained at each of the four temperatures, four heating times were chosen for the analysis of the polymers and total oxidation products. Significant linear relationships were found between polymer contents and total oxidation product contents. The contents of polymers and their linkage types were analyzed by High Performance Size Exclusion Chromatography. The polymers formed at four temperatures were qualitatively identified as dimers. The dimers with peroxide linkages were detected from methyl linoleate oxidized at $60^{\circ}C\;and\;90^{\circ}C$ but they were not detected from methyl linoleate oxidized at $120^{\circ}C\;and\;150^{\circ}C$. Therefore, all dimers formed at $120^{\circ}C\;and\;150^{\circ}C$ seemed to be the ones with ether linkage or carbon to carbon linkage. The degradation rate of the dimers with peroxide linkages at $90^{\circ}C$ was faster than at $60^{\circ}C$.

• Journal of the Korean Chemical Society
• /
• v.45 no.4
• /
• pp.312-317
• /
• 2001

7'-Aldehyde-nucleosides analogue (2a, 2c) were synthesized from 6-N-benzoyl-2',3'-O-isopropylideneadenosine and uridine. The condensation of 2 with ethoxycarbonylmethylene Wittig reagent produced the adenosine and uridine analogues containing extended conjugated diene and ethoxycarbonyl group, ethyl-1',5',6',7',8'-pentadeoxy-1'-(adenin-9-yl)-$\beta$-D-ribo-nona-5'(E),7'(E)-dienofuranuronate (4b) and ethyl-1'. 5',6',7',8'-pentadeoxy-1'-(uracil-1-yl)-$\beta$-D-ribo-nona-5'(E),7'-(E)-dienofuranuronate (4c). 9-[8',8'-dibromo-5',6',7',8' -tetradeoxy-$\beta$-D-ribo-octa-5'(E),7'(E)-diene]nucleosides (6b, 6c) were also prepared from 2 with similar method.

• Proceeding of EDISON Challenge
• /
• 2015.03a
• /
• pp.147-150
• /
• 2015

Polynitrogen Compounds (PNC)는 질소만으로 이루어진 물질을 칭하며, 주로 질소간의 단일 결합과 이중결합으로 이루어져 있다. 질소 간 단일결합에너지 38.4kcal/mole에 비해 유난히 큰 229kcal/mole의 삼중결합 에너지 덕택에 PNC는 고에너지 물질로 큰 각광을 받고 있다. PNC는 합성과정이 큰 흡열반응으로 실험이 까다로워 이론적인 연구가 많이 진행되어왔다. 그 중에서 고리형태의 $N_5{^-}$가 안정할 것으로 예측되며, 실험적으로도 발견되었다. $N_5{^-}$를 안정화시키기 위해 많은 연구가 진행되었으며 그 중 하나가 금속과의 결합을 통한 화합물의 안정화이다. 본 연구에서는 $N_5{^-}$와 Cyclopentadienyl($C_5H_5{^-}$)이 전자구조나 기하학적 구조가 매우 유사함에 착안하여 이미 상대적으로 많은 합성이 보고되어 있는 $M(C_5H_5)_3$, $M(C_5H_5)_4$의 전이금속 M구조에 대하여 아직 발견되지 않은 $M(N_5)_3$, $M(N_5)_4$ 화합물의 구조와 열역학적 안정성을 알아보도록 한다. 본 연구에서 찾아진 $Zr(C_5H_5)_4$은 현재까지 실험적으로 보고된 $M(C_7H_7)(C_5H_5)$ 클러스터 구조에 비해 질소함유량이 약 67% 더 높다.

• Journal of Life Science
• /
• v.7 no.3
• /
• pp.167-171
• /
• 1997

As an initial effort to elucidate RNA: protein binding in a way to regulate translation initiation and phosphorylation, a cDNA encoding a double-stranded RNA binding factor (RBFII)was isolated from Hela ZAPII cDNA library by affinity screening using [$\alpha$$^{-32}$P] UMP-labeled HIV Rev-responsive element(RRE) RNA. The nucleotide sequence of RBF (or TRBP) cDNA except the 5’end. At the 5’end, This common ORF was fused in-frame to N-terminal residues of Lac-Z through a unique 138 nt sequence encoding 46residues in the case of RBFII and a 63 nt sequence encoding 21 residuces in the case of RBFI. The context of ATG appearing first in the sequences suggests that both these cDNA inserts are incomplete at the 5’end.

• Journal of the Institute of Electronics Engineers of Korea SD
• /
• v.43 no.2 s.344
• /
• pp.13-17
• /
• 2006

Pentacene channel for organic thin film transistor was deposited on the SiOC film by thermal evaporation. The growth of pentacene is related with the Diels-Alder reaction and the nucleophilic reaction by the thermal induction. The surface is an important factor to control the recursive Diels-Alder reaction for growing of pentacene on SiOC far The terminal C=C double bond of pentacene molecule was broken easily as a result of attack of the nucleophilic reagents on the surface of SiOC film. The nucleophilic reaction can be accelerated by increasing temperature on surface, and it maks pentacene to grow hardly on the SiOC film with a flow rate ratio of $O_2/(BTMSM+O_2)=0.5$ due to its inorganic property. The nucleophlic reaction mechanism is $SN_2(bimolecular nucleophilic substitution)$ type.

• Journal of the Korean Society of Industry Convergence
• /
• v.6 no.1
• /
• pp.17-21
• /
• 2003

5원환 고리아세탈 화합물인 4-methylenes(4,5)을 합성하고 저온조건 하에서 중합반응을 조사한 결과, 선택적인 개환중합이 일어났다. 보통의 양이온 개시제를 사용한 결과 $-78^{\circ}C$에서 가교체가 얻어졌으며, $CH_3SO_3H$를 개시제로 사용하면 같은 조건에서도 주사슬과 곁사슬에 이중결합을 가지는 개환중합체가 얻어진다. 이 중합체는 반응성을 가지는 불포화기를 포함하고 있으므로 prepolymer로써 널리 사용될 수 있다.