光谱学与光谱分析
光譜學與光譜分析
광보학여광보분석
SPECTROSCOPY AND SPECTRAL ANALYSIS
2015年
8期
2292-2296
,共5页
夏道成%李万程%李洁筠%王改萍%段宏伟%任旭文%冯凯%李佩陶%王慧芳%蒲改琴
夏道成%李萬程%李潔筠%王改萍%段宏偉%任旭文%馮凱%李珮陶%王慧芳%蒲改琴
하도성%리만정%리길균%왕개평%단굉위%임욱문%풍개%리패도%왕혜방%포개금
3,6-二羟基邻苯二腈%丙二酸%金属酞菁配合物%合成
3,6-二羥基鄰苯二腈%丙二痠%金屬酞菁配閤物%閤成
3,6-이간기린분이정%병이산%금속태정배합물%합성
3,6-dihydroxy phthalonitrile%Malonate%Metal phthalocyanine complexes%Synthesis%Characterization
对新型取代基酞菁和酞菁晶体合成和性质进行了研究。因为酞菁在信息、医疗、化工等众多领域有很广泛的应用,所以近百年来一直是科学家研究的热点课题。酞菁经过近百年的研究,科学家已经合成了上万种酞菁衍生物,但是,随着科技的不断进步,人类社会不断发展的需求,具有新特性的新型酞菁的获得仍是相关科技工作者孜孜以求的目标。为此,在本论文中,我们改进了合成方法,合成了新型的桥联酞菁材料:1,11,15,25‐四羟基‐4,8,18,22‐二(桥联二丙羧基)酞菁铜,表征其结构。并研究电化学性质。首先以丙二酸和3,6‐二羟基邻苯二腈为起始原料,以水为溶剂,加入浓硫酸作为催化剂,先合成前体,即丙二酸3,3′‐二(6–羟基邻苯二腈)脂。然后再用丙二酸3,3′‐二(6‐羟基邻苯二腈)脂与一水合乙酸铜,以正戊醇为溶剂,以DBU为催化剂,合成了1,11,15,25‐四羟基‐4,8,18,22‐二(桥联二丙羧基)酞菁铜,其分子式是C38 H16 N8 O12 Cu。对1,11,15,25‐四羟基‐4,8,18,22–二(桥联二丙羧基)酞菁铜进行紫外吸收及荧光光谱测定,证明合成产物是目标产物,并研究了1,11,15,25‐四羟基‐4,8,18,22‐二(桥联二丙羧基)酞菁铜的电化学性质。
對新型取代基酞菁和酞菁晶體閤成和性質進行瞭研究。因為酞菁在信息、醫療、化工等衆多領域有很廣汎的應用,所以近百年來一直是科學傢研究的熱點課題。酞菁經過近百年的研究,科學傢已經閤成瞭上萬種酞菁衍生物,但是,隨著科技的不斷進步,人類社會不斷髮展的需求,具有新特性的新型酞菁的穫得仍是相關科技工作者孜孜以求的目標。為此,在本論文中,我們改進瞭閤成方法,閤成瞭新型的橋聯酞菁材料:1,11,15,25‐四羥基‐4,8,18,22‐二(橋聯二丙羧基)酞菁銅,錶徵其結構。併研究電化學性質。首先以丙二痠和3,6‐二羥基鄰苯二腈為起始原料,以水為溶劑,加入濃硫痠作為催化劑,先閤成前體,即丙二痠3,3′‐二(6–羥基鄰苯二腈)脂。然後再用丙二痠3,3′‐二(6‐羥基鄰苯二腈)脂與一水閤乙痠銅,以正戊醇為溶劑,以DBU為催化劑,閤成瞭1,11,15,25‐四羥基‐4,8,18,22‐二(橋聯二丙羧基)酞菁銅,其分子式是C38 H16 N8 O12 Cu。對1,11,15,25‐四羥基‐4,8,18,22–二(橋聯二丙羧基)酞菁銅進行紫外吸收及熒光光譜測定,證明閤成產物是目標產物,併研究瞭1,11,15,25‐四羥基‐4,8,18,22‐二(橋聯二丙羧基)酞菁銅的電化學性質。
대신형취대기태정화태정정체합성화성질진행료연구。인위태정재신식、의료、화공등음다영역유흔엄범적응용,소이근백년래일직시과학가연구적열점과제。태정경과근백년적연구,과학가이경합성료상만충태정연생물,단시,수착과기적불단진보,인류사회불단발전적수구,구유신특성적신형태정적획득잉시상관과기공작자자자이구적목표。위차,재본논문중,아문개진료합성방법,합성료신형적교련태정재료:1,11,15,25‐사간기‐4,8,18,22‐이(교련이병최기)태정동,표정기결구。병연구전화학성질。수선이병이산화3,6‐이간기린분이정위기시원료,이수위용제,가입농류산작위최화제,선합성전체,즉병이산3,3′‐이(6–간기린분이정)지。연후재용병이산3,3′‐이(6‐간기린분이정)지여일수합을산동,이정무순위용제,이DBU위최화제,합성료1,11,15,25‐사간기‐4,8,18,22‐이(교련이병최기)태정동,기분자식시C38 H16 N8 O12 Cu。대1,11,15,25‐사간기‐4,8,18,22–이(교련이병최기)태정동진행자외흡수급형광광보측정,증명합성산물시목표산물,병연구료1,11,15,25‐사간기‐4,8,18,22‐이(교련이병최기)태정동적전화학성질。
In this dissertation ,we study the synthesis and character of new substituted Phthalocyanine .Due to the widely appli‐cation of Pcs in the fields ,such as the communication ,medical treatment ,chemical industry and so on ,therefore ,they have been a hot topic over several decades by scientists .Nowadays ,scientists have prepared thousands of Pcs and their derivatives . However ,along with the human society development and the progress in science and technology ,the new phthalocyanine with novle characteristics are still the goal of the scientists .In this dissertion ,the synthetic methods of the phthlocyanine is im‐proved .The synthesis and characterization of 1 ,11 ,15 ,25‐tetrahydroxy‐4 ,8 ,18 ,22‐di(bridged dipropionate carboxyl) phthalocy‐anines are reported in this paper .The mixtures of malonic acid and 3 ,6‐dihydroxy‐phthalonitrile was added to water under stiri‐ing .Then ,a catalyst amount of sulfuric acid was added .The first synthetic precursor ,i .e .,malonic acid 3 ,3′‐bis(6‐hydroxy phthalonitrile) butter ,its molecular formula is C19 H8 N4 O6 .phthalocyanines was prepared by malonic acid 3 ,3′‐bis(6‐hydroxy phthalonitrile) butter and dihydrate zinc acetate ,copper acetate monohydrate in n‐amyl alcohol ,using DBU as a catalyst under the 135 ℃ ,molecular formula of phthalocyanine complexes is C38 H16 N8 O12 M .The product was characterized by Ultraviolet‐vis‐ible (UV/Vis) Spectrum absorption and fluorescence ,The results are agreement with the proposed structures .And electro‐chemical properties were studied .