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Received October 30, 2010
Accepted March 14, 2011
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자기조립단분자막을 위한 보편적이고 기능화된 긴 사슬 알킬티올 연결자의 제조

Preparations of Universal, Functionalized Long-Chain Alkylthiol Linkers for Self-assembled Monolayers

1전북대학교 수소·연료전지공학과 특성화대학원, 561-756 전북 전주시 덕진동 1가 664-14 2(주)에스텍파마 부설연구소, 445-938 경기도 화성시 향남읍 하길리 1407-9 3전북대학교 반도체·화학공학부, 반도체물성연구센터, 561-756 전북 전주시 덕진동 1가 664-14
1Department of Hydrogen and Fuel Cells Engineering, Specialized Graduate School, Chonbuk National University, 664-14 1 ga, Duckjin-dong, Duckjin-gu, Jeonju-si, Jeonbuk 561-756, Korea 2EstechPharma Co., Ltd., 1407-9 Hagil-ri, Hyangnam-eup, Hwaseong-si, Gyeonggi 445-922, Korea 3School of Semiconductor and Chemical Engineering and Technology, and Semiconductor physics Research Center, Chonbuk National University, 664-14 1 ga, Duckjin-dong, Duckjin-gu, Jeonju-si, Jeonbuk 561-756, Korea
Korean Chemical Engineering Research, June 2011, 49(3), 330-337(8), NONE Epub 8 June 2011
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Abstract

본 연구에서는 자기조립단분자막(SAM)의 연구에 유용한 일련의 ω-mercapto alkyl amine 1 및 ω-mercapto alkanoic acid 2를 만드는 제조공정을 서술하였다. 먼저 첫 번째 목표물질인 ω-mercapto alkyl amine 1의 제조방법은 다음과 같다: 먼저 시중에서 시판되는 potassium phthalimide와 ω-bromo alcohol을 80℃ , DMF 용매에서 치환반응으로 화합물3을 합성하였다. 아민기와 알코올기를 포함하는 화합물 4을 합성하기 위하여 먼저 화합물 3를 hydrazine hydrate로 환류시킨 후, 이어서 c-HCl로 처리하여 부반응물 5를 수반하여 생성물 4를 76~98% 수율로 만들었다. ω-aminoakanol 4의 hydroxyl기를 HBr로 브로민화반응을 하여 ω-bromoamine 화합물 6을 34~97% 수율로 만들었다. 티올기를 도입하_x000D_ 기 위하여 화합물 6을 95% 에탄올 속에서 thiourea와 치환 반응하여 ω-aminoalkanthiuronium 7을 만든 다음, 이 화합물을 센 염기(KOH)와 센 산으로 처리하여 목표화합물, ω-mercapto alkylamines 1을 총 5단계를 걸쳐서 제조하였다. 덧붙여 두 번째 목표물질인 ω-mercapto alkanoic acid 2는 다음과 같이 2단계를 통하여 제조하였다: ω-bromo alkanoic acid를 95% 에탄올 속에서 thiourea로 처리하여 화합물 7을 만든 다음, 센 염기(KOH)를 처리하여 thiuronium bromide를 제거한 후, 다시 센 산(HCl) 수용액으로 처리하여 두 번째 목표화합물 ω-mercapto alkanoic acid 2을 얻었다. 제조한 긴 사슬 알킬티올 1과 2 유도체들은 금속(Au, Pt, Ti)에 자기조립단분자 막을 형성함으로써 단백질, 효소 및 다양한 생체분자를 고정하는 연결자로 사용될 수 있으며, 그 밖에 금속의 표면개질을 이용하여 다양한 응용 연구를 위한 화학 도구로 사용될 수 있다.
In this research, the preparation processes for making a series of ω-mercapto alkylamine 1 and ω-mercapto alkanoic acid 2 useful for studying of the self-assembled monolayer(SAM) are described. The preparation methods of the first goal materials, ω-mercapto alkylamines 1 were carried out as follows: First, ω-phthalimide alkanol 3 was synthesized from commercially available potassium phthalimide derivatives and ω-bromoalkanol in DMF at 80℃ via substitution reaction. After refluxing ω-phthalimide alkanol 3 with hydrazine hydrate in ethanol followed by treating with c-HCl, ω-aminoalkanol 4 was obtained in 76~98% yield, accompanied with side-product 5. Bromination of hydroxyl moiety of ω-aminoalkanol 4 using aqueous hydrobromic acid furnished ω-bromoamine 6 in 34~97% yields. Substitution reaction 6 with thiourea in 95% ethanol gave ω-aminoalkanthiuronium 7, which was treated with aqueous strong base and aqueous strong sulfuric acid gave desired products, ω-mercapto alkylamines 1 through overall 5 steps._x000D_ The second target material, ω-mercapto alkanoic acid 2 was prepared via 2 steps. ω-bromo alkanoic acid was reacted with thiourea to give ω-thiourea alkanoic acid 7 in 69-85%, which was treated with aqueous strong base and strong acid to furnish ω-mercapto alkanoic acid 2 in 50~98%. The fabricated long-chain alkylthiol(LCAT) can be used as linkers to immobilize protein, enzyme and various kinds of biomolecules on the surface of metallic materials(Au, Pt, Ti) by SAM, and can be useful chemical tools for the application study on the surface modification of metallic materials.

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