Abstract:
본 발명은 디아릴에텐 유도체와 이를 이용한 광변색 박막에 관한 것으로서, 더욱 상세하게는 결정이나 응집이 잘 일어나지 않는 디아릴에텐 유도체를 기판 위에 증착시켜 박막을 제조함으로써, 종래 광변색 화합물 외에 수지 등이 혼합된 박막과 달리 고농도의 광변색 화합물로 구성될 수 있어 나노미터 수준까지 광변색 효과를 유도할 수 있을 뿐 아니라 균일한 감도를 나타내며, 기존의 증착 방법에 비해 작업성이 향상될 뿐 아니라 투광성이 우수하고 가역적으로 광신호를 제어할 수 있어 광에 의한 색변화, 정보의 기록 및 광신호의 전달 매체로 널리 활용될 수 있는 디아릴에텐 유도체와 이를 이용한 광변색 박막에 관한 것이다.
Abstract:
PURPOSE: A process for preparing epothilone derivatives is provided, thereby preparing epothilone derivatives having improved anticancer activity in higher purity and yield, so that the process can be useful for development of anticancer drugs having improved activity. CONSTITUTION: The process for preparing epothilone derivatives of formula (1b) comprises the steps of: (i) aldol condensation reacting ketonic acid derivative of formula (2) with phenylsulfone substituted aldehyde derivative of formula (3) to prepare phenylsulfone substituted hydroxy ketonic acid derivative of formula (4); (ii) removing phenylsulfone(-SO2Ph) from the compound of formula (4) to prepare hydroxy ketonic acid derivative of formula (5) with stereo selectivity; (iii) reacting the compound of formula (5) with thiazole alcohol derivative of formula (6) to prepare ester derivative of formula (7); (iv) double bond binding reaction of the compound of formula (7) using Grubbs catalyst to remove a protecting group(TBS), thereby preparing deoxyepothilone compound of formula (1a); and (v) epoxidation of the deoxyepothilone compound of formula (1a).
Abstract:
PURPOSE: Provided are sulfur-containing acrylic or methacrylic compounds of general formula 1 and a preparation method thereof, which can give plastic materials improved in transparency, heat resistance, hardness, as well as refractive index and abbe value, thus they are suitable to use in highly integrated optical parts. CONSTITUTION: The sulfur-containing acrylic or methacrylic compounds are represented by general formula 1, wherein each R1 and R6 is independently H or -CH3; X1 is -O-, -S-, -SO2-, -C(=O)-, and formula 1-1; each a and b is an integer ranging from 0 to 2, provided that they satisfies a+b=2; each R2 and R5 is independently (CH2)n1-O, (CH2CH2O)n2 or -(CH-CH2-O)n3-, wherein the oxygen atom is connected to the C=O side; each R3, R4 and R12 is independently, -C6H4-, -(CH2)n4-, -(CH2)n6-(SCH2CH2)n5-, -C6H4-CH2- or -CH2S-C6H4-CH2, or when X1 is -P=SR7-, R3 and R4 are -CH2CH2O-, -(CH2)n9-(CH2CH2S)n10- or -C6H4S, wherein the benzene ring is connected to -SCO- side; R7 is (C1-C20)alkylthio ether, -O-C6H4-S0CH3, -O-C6H4-OCH3 or -C6H4-C6H5; each R8 and R9 is independently linear (C1-C20)alkyl or (C3-C10)cyclic alkyl, phenyl, -CH2-C6H5 or CF3; each R10 and R11 is H, (C1-C20)alkyl, (C3-C10)cyclic alkyl, phenyl or benzyl, or linked together with N to form (C3-C10)cyclic amine; each X2 and X3 is a bond, or S or O; each of n1 to n4, and n6 is an integer ranging from 0 to 20; each n5, n7, and n9 is an integer of 0 to 10; and each n8 and n10 is an integer of 1 to 10.
Abstract:
본 발명은 에포싸일론 유도체의 제조방법에 관한 것으로서, 더욱 상세하게는 알돌축합 반응에 사용되어지는 알데하이드 화합물과 케톤 화합물의 구조를 특이성 있게 고안하여 반응에 사용함으로써 부분이성질체 중 원하는 이성질체의 비율이 절대적으로 우위에 있도록 합성하여 용이하게 이성질체를 분리할 수 있도록 하는 등의 일련의 제조방법의 특징으로 인하여 차세대 항암제로 유력한 에포싸일론(Epothilone) 유도체를 고 순도 및 고 수율로 전합성하는 제조방법에 관한 것이다.
Abstract:
PURPOSE: A method for preparing a photochromic plastic lens is provided, to obtain a photochromic plastic lens which has good refractive index, surface hardness and photochromism lifetime and whose refractive index can be controlled widely by the change of the composition, by varying the curing temperature and time. CONSTITUTION: The method comprises leaving a photochromic resin composition at a temperature of a room temperature to 70 deg.C for 30-360 min to initiate the degradation reaction of an initiator; maintaining the temperature at 70-80 deg.C for 110-180 in; maintaining the temperature at 85-95 deg.C for 110-130 min; maintaining the temperature at 110-130 deg.C for 30-240 min; and cooling the thermally cured one naturally. The photochromic resin composition comprises 100 parts by weight of at least one monomer selected from the aromatic radical polymerizable monomers represented by the formula 1; 0.001-90 parts by weight of at least one photochromic compound selected from the group consisting of diarylethene-based one, Spirobenzopyran-based one and diazo-based one absorbing the light with the wavelength of 250 nm or more; and 0.1-10 parts by weight of a photoinitiator.
Abstract:
PURPOSE: Provided are diarylethene derivatives to which crystallization or condensation hardly happens and a photochromic thin film using the same by depositing the diarylethene derivatives on a base plate. Therefore the thin film induces photochromic effect on nanometers level, has regular sensitivity and excellent light transmission, and controls photosignals. CONSTITUTION: The photochromic diarylethene derivative is represented by the formula(1), wherein R1 is a binding line, a C1-C3 alkylene group or a fluorine substituted C1-C3 alkylene group, Ar¬1 and Ar¬2 are individually represented by the formula(2) or (3), and Z is a fluorine substituted or unsubstituted methylene group or carbonyl group. The photochromic thin film is manufactured by depositing the compound of the formula(1) on a base plate.
Abstract:
PURPOSE: Provided is a process for preparing pyridone derivative represented by the formula(1) and useful as a therapeutics of Alzheimer's disease(AD). CONSTITUTION: The process for preparing pyridione derivative of the formula(1) comprises the steps of; reacting 1,4-cyclohexanedione monoketal of the formula(2) with secondary amine under acid catalyst; then treating the resultant with propiolamide of the formula(3) to obtain the compound of the formula(1). In the formulae, R1 and R2 represent individually C1-C6 alkyl group or R1 and R2 bind together to form 5-8 membered hetero ring.
Abstract:
PURPOSE: Provided is a photochromic resin composition excellent in refraction rate, surface hardness, and repeatability of photo-discoloration, which can be used for functional optical lenses, filters, imaging, display elements or photonic integrated elements, photo discs, or optically recording media. CONSTITUTION: The photochromic resin composition contains: 100pts.wt. of at least one kind of monomer selected from aromatic radical polymerizable monomers represented by the formula 1; 0.001-90pts.wt. of at least one photochromic compound selected from the group consisting of a diarylethene, a spirobenzopyran, and a diazo, which has an absorption-wavelength of 250nm or more; 0.1-10pts.wt. of a photo-initiator such as 2,2'-azobis isobutyro nitrile(AIBN) and benzoyl peroxide(BPO). In the formula, R1 and R2 are identically or differently H or C1-C4 alkyl, R3 and R4 are the same as the R1 and R2 or C1-C4 haloalkyl, R5 is H, C1-C4 alkyl, and etc., Z is a direct bond, -S-, or -O-, Y is a direct bond, -S-, -SO2-, -O-C(=O)-, and etc., X is H, -O-, -S-, -SO2-, and etc., k is 0 or 1, l is 1 or 2, m is 0, 1, or 2, and n is 0 or an integer of 1-20.