• Restorative Dentistry and Endodontics
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• 제32권3호
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• pp.208-221
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• 2007

파괴 인성 실험은 상아질-복합레진 계면의 파절 저항성을 평가할 수 있는 임상적으로 신뢰 할 만한 방법이다. 본 연구의 목적은 상아질-레진 계면의 파괴인성과 미세인장결합강도를 측정하여 이 두 실험방법이 상아질-레진 결합을 평가하는 데 가지는 유용성을 비교, 평가하는 것이다 파괴 인성 측정에는 short-rod 시편 형태를 이용하였다. 각 시편에서는 소의 하악절치에서 절단한 치아 절편을 포함시켜 결합면을 얻었다. 미세인장 결합강도 또한 소의 하악절치 순면을 연마하여 상아질을 노출시킨 후 상아질 접착제를 도포하고 레진 블록을 축조하여 측정하였다. 각 시편들은 $37^{\circ}C$ 증류수에 24시간 보관한 후 각 실험방법에 맞게 인장력을 가하여 측정치를 구하였다. 통계분석은 95% 신뢰수준의 ANOVA와 Tukey's test를 이용하였으며, 두 실험방법의 상관관계를 보기 위해 Pearson's 상관계수를 계산하였다. 전자현미경 검사를 통해 미세구조 또한 관찰하여 다음과 같은 결론을 얻었다. 1. 파괴인성은 SE군이 가장 높은 값을 나타냈으며, Adper Single Bond 2 (SB), OptiBond Solo (OB) ONE-STEP PLUS (OS), ScotchBond Multi-purpose (SM)군 순으로 나타났고, Clearfil SE Bond (SE)군은 다른 실험군에 비해 유의하게 높은 값을 나타내었으나 (p <0.05), 다른 실험군 사이에는 유의차가 없었다 (p > 0.05). 2. 미세인장결합강도는 SE군이 가장 높은 값을 나타냈으며, SB, OB, SM, 그리고 OS 순으로 나타났다. SB, OB, SM, SE군 사이에는 통계학적인 유의차가 없었으나 (p > 0.05), OS군의 미세인장결합강도는 다른 4개의 실험군에 비해 낮은 값을 나타내었다 (p < 0.05). 3. FE-SEM관찰에서 피막도가 두껍게 나타난 SM군, SE군과 피막도가 얇은 OS군, OB군, SB군 간에 파괴양상이 다르게 나타났다 즉 전자는 접착층 내 파괴가 일어난 반면, 후자는 resin tag나 레진 침투층 내에서 파절되는 양상을 나타내었다. 4. 파괴 인성과 미세인장결합강도 사이에는 통계학적으로 유의 한 상관 관계가 없었다 ($r^2=0.223$, t=0.927). 이와 같은 결과를 토대로, 상아질 접착제의 임상적 효율성을 평가하고자 할 때는 결합강도 뿐만 아니라. 파괴인성도 함께 고려하여 임상적용의 예견성을 높여야 한다고 결론내릴 수 있다.

• Environmental Analysis Health and Toxicology
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• 제14권1_2호
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• pp.65-73
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• 1999

Dioxins refer to a family of chemicals comprising 75 polychlorinated dibenzo-p-dioxin (PCDD) and 135 polychlorinated dibenzo-p-furan (PCDF) congeners, which may cause skin disorder, human immune system disruption, birth defects, severe hormonal imbalance, and cancer. The effects of exposure of dioxin-like compounds such as PCBs are mediated by binding to the aryl hydrocarbon receptor (AHR), which is a ligand-activated transcription factor. To grasp physicochemical factors affecting human toxicity of dioxins, six geometrical and topological indices, eleven thermodynamic variables, and quantum mechanical descriptors including ESP (electrostatic potential) were analyzed using QSAR and semi-empirical AM1 method. Planar dioxins with high lipophilicity and large surface tension show the probability that negative electrostatic potential in the lateral oxygen may make hydrogen bonding with DNA bases to be a carcinogen.

• 한국고분자학회:학술대회논문집
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• 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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• pp.347-347
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• 2006

Polymers containing poly(vinyl phosphonic) acid segments are promising candidates to be used as proton conducting membranes. Solid state NMR spectroscopy represents an ideal probe of proton motion on the molecular level, because it allows us to selectively detect the nuclei of interest. In this paper, we apply solid state NMR methods to poly(vinyl phosphonic) acid in order to demonstrate that the proton conduction of poly(vinyl phosphonic acid) results from P-OH proton through hydrogen bonding and that the condensation of phosphonic acid leads to decrease in proton conductivity. $^{1}H\;and\;^{31}P$ solid state NMR experiments are supported by quantum chemical computation of NMR parameters.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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• pp.529-529
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• 2012

Dispersion of carbon nanotubes in biocompatible media are of particular interest for diverse biomedical and nanomedicine applications. Various biomolecules and biopolymers such as DNA, proteins, poly L-lysine, starch, gelatin, steroid biosurfactants, and chitosan have shown capability for the effective dispersion of carbon nanotubes in water. Chitosan has demonstrated capacity for effective dispersion of single-walled carbon nanotubes (SWCNTs) in acidic medium and it also showed tendency to preferentially disperse smaller diameter nanotubes. Chemical functionalizations of chitosan enable its solubility in neutral pH water by reducing the intra and inter molecular hydrogen bonding. Herein, we present a neutral pH water soluble chitosan derivative, chitosan-hydroxyphenyl acetamide (CHPA), obtained by functionalizing the amino groups of chitosan with 4-hydroxyphenyl acetic acid, as an efficient biocompatible dispersant for debundling and solubilization of SWNTs in neutral aqueous solutions. Various process conditions for individual dispersion of SWCNTs are analyzed based on optical absorption and Raman spectroscopy.

• 통합자연과학논문집
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• 제9권3호
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• pp.161-165
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• 2016

The p21-activated kinase-1 (PAK1) has emerged as a potential target for anticancer therapy. It is overexpressed in ovarian, breast and bladder cancers. This suggests that PAK1 may contribute to tumorigenesis. 4-azaindole derivatives are reported as potent PAK1 inhibitors. The present work deals with the molecular docking studies of 4-azaindoles with PAK1. Probable binding mode of these inhibitors has been identified by molecular modeling. Docking results indicated that hydrogen bonding interactions with Glu345 and Leu347 are responsible for governing inhibitor potency of the compounds. Additionally, Val284, Val328, Met344 and Leu396 were found to be accountable for hydrophobic interactions inside the active site of PAK1.

• 대한화학회지
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• 제32권3호
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• pp.243-248
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• 1988

수용액에서 몇가지 란탄 착화합물의 hypersensitive 전이대를 연구하였다. 리간드의 염기도$(pK_a)$와 란탄 착화합물의 hypersensitive 전이대의 진동자 세기 사이에 정립된 선형 관계에 근거를 두고, 금속-리간드 결합간에 존재하는 공유 결합성을 anthranilate, pyrazine-2-carboxylate, 및 pyruvate 착화합물에 대해서 논하였다.

• Bulletin of the Korean Chemical Society
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• 제27권11호
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• pp.1737-1740
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• 2006

The optimized structures and complexation energies of bis(18-crown-6-ether) analogue (2) of Trgers base (1) with a series of primary alkylbisammonium ions have been calculated by DFT B3LYP/6-31G(d,p) method. The calculated complexation efficiency (-142.84 kcal/mol) of 2 for butane-1,4-diylbisammonium guest is better than twice of the value (-61.40 kcal/mol) for butylammonium ion. The multiple hydrogen-bond abilities for the complexes are described as the function of the length of the alkyl substituents of the bisammonium guests with normal-alkyl chain [$-(CH_2)_{n-}$, n = 4-8]. The longer bisammonium guest shows the stronger hydrogen-bonding characterizations (the distance and the quasi-linear angle of the N-H…O) to the host 2 than the shorter bisammonium ions. These calculated results agree with the experimental data of the complexation of 2 with bisammonium salts ([$NH_3(CH_2)_nNH_3$] $Cl_2$).

• 한국생물물리학회:학술대회논문집
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• 한국생물물리학회 1999년도 학술발표회 진행표 및 논문초록
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• pp.36-36
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• 1999

Bacterial Δ-3-ketosteroid isomerase (KSI) catalyzes the conversion of Δ-to Δ-3-ketosteroids via enolate formation, which is also found in the synthesis of all steroid hormones in mammals. In Pseudomonas testosteroni, KSI Asp38 (pKa ~ 4.7) was identified as the general base which abstracts the steroid C4b-H (pKa ~ 12.7) to form the dienolate intermediate.(omitted)

• Bulletin of the Korean Chemical Society
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• 제21권8호
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• pp.813-816
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• 2000

The synthesis of bisphenol A-derived calixarenes has been studied by changing the protecting group of the phe-nol moiety and reaction conditions. Depending on the protecting groups,the corresponding calix[6,7,8]arenes are obtained in different rat ios. For example, whcn mono-p-tert-butyldimethylsilyl-protected bisphenol A is treated with paraformaldehyde and a catalytic amount ofaqueous KOH in refluxing p-xylene with a Dean-Stark water collector for 36 h, the corresponding calix[8]arene, calix[7]arene, and calix[6]arene are producedand separated in the ratio of about 3 : 2 : l and with overall 63% yield. The calixarenes are characterized by NMR spectroscopy and mass analysis. The X-raycrystal structure of the calix[8]arene shows a pleated loop confor-mation, stabilized by intramoIecular hydrogen bonding between the inner phenolic hydroxy groups.

• Bulletin of the Korean Chemical Society
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• 제19권9호
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• pp.980-985
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• 1998

The excited-state intramolecular proton transfer (ESIPT) emission has been observed for 0.01 mM p-aminosalicylic acid (AS) in nonpolar aprotic solvents as demonstrated by the large Stokes' shifted fluorescence emission around 440 nm in addition to the normal emission at 330 nm. However in aprotic polar solvent such as acetonitrile, the large Stokes' shifted emission band becomes broadened, indicating existence of another emission band originated from intramolecular charge transfer (ICT). It is noteworthy that in protic solvents such as methanol and ethanol the normal and ICT emissions are quenched as the AS concentration decreases, followed by the appearance of new emission at 380 nm. These results are interpreted in terms of ESIPT coupled charge transfer in AS. Being consistent with these steady-state spectroscopic results, the picosecond time-resolved fluorescence study unravelled the decay dynamics of the ESIPT and ICT state ca. 300 ps and ca. 150 ps, respectively with ca. 40 ps for the relaxation time to form the ICT state.