CN106278938A - 一类水溶性双希夫碱钾盐的合成与应用 - Google Patents

一类水溶性双希夫碱钾盐的合成与应用 Download PDF

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CN106278938A
CN106278938A CN201610658625.6A CN201610658625A CN106278938A CN 106278938 A CN106278938 A CN 106278938A CN 201610658625 A CN201610658625 A CN 201610658625A CN 106278938 A CN106278938 A CN 106278938A
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base
subunit
corrosion inhibiter
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water solublity
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苏纪宏
王震强
丁戈
高放
李红茹
张胜涛
罗自萍
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Chongqing University
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C249/00Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C249/02Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of compounds containing imino groups
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
    • C23F11/14Nitrogen-containing compounds
    • C23F11/146Nitrogen-containing compounds containing a multiple nitrogen-to-carbon bond

Abstract

一类水溶性双希夫碱钾盐作为铜的缓蚀剂,其化学结构式如下:其中结构式中C1,R1=‑OK,R2=R3=H;C2,R2=‑OK,R1=R3=H;C3,R3=‑OK,R1=R2=H.本发明的一类水溶性双希夫碱钾盐的缓蚀剂在质量比为3.5%的氯化钠溶液中对金属铜有缓蚀作用;由于有机盐的化学结构,大大提高了缓蚀剂的水溶性,从而有助于提高缓蚀剂的缓蚀效应;且合成及分离方法简单,原料方便易得。

Description

一类水溶性双希夫碱钾盐的合成与应用
技术领域
本发明属于希夫碱类缓蚀剂及合成技术领域,特别涉及水溶性双希夫碱钾盐及其合成与在质量比为3.5%的氯化钠溶液中对铜的缓蚀应用。
背景技术
现有的希夫碱类缓蚀剂以及其他类型的缓蚀剂在质量比为3.5%的氯化钠溶液中对铜具有一定的缓蚀作用,但缓释效应偏低,主要是有机缓蚀剂在氯化钠溶液中的溶解度极低,无法达到高浓度的缓释溶液对铜表面形成多层吸附。
发明内容
本发明的目的就是为了克服上述背景技术的不足,合成一类水溶性双希夫碱钾盐,作为在质量比为3.5%的氯化钠溶液中金属铜的缓蚀剂。
本发明所涉及的一类水溶性双希夫碱钾盐的缓蚀剂,其化学结构式如下:
其中结构式中C1,R1=-OK,R2=R3=H;C2,R2=-OK,R1=R3=H;C3,R3=-OK,R1=R2=H.
上述水溶性双希夫碱钾盐的合成方法,步骤如下:
将2,2'-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯酚与氢氧化钾以摩尔比为1:2.2加入50mL单口烧瓶,加入体积为2,2'-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯酚8~10倍的无水乙醇,常温磁力搅拌2小时,反应结束,减压蒸馏除去溶剂,然后用二氯甲烷萃取,减压蒸馏,得到权利要求1的化合物。
其中结构式中C1,R1=-OK,R2=R3=H;C2,R2=-OK,R1=R3=H;C3,R3=-OK,R1=R2=H.
本发明的水溶性双希夫碱钾盐的缓蚀剂在质量比为3.5%的氯化钠溶液中对金属铜具有缓蚀作用;水溶性好,对铜表面能够充分有效的进行吸附;且合成及分离方法简单,原料方便易得。
附图说明
图1.本发明实施例1中2,2'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯醇酸钾的1H核磁共振谱图。
图2.本发明实施例1中3,3'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯醇酸钾的1H核磁共振谱图。
图3.本发明实施例1中4,4'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯醇酸钾的1H核磁共振谱图。
具体实施方式
下面结合实例和附图进一步说明本发明:
实施例1
2,2'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯醇酸钾的合成
2,2'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯酚(1.00g,2.4mmol)、氢氧化钾(0.29g,5.3mmol)加入50mL单口烧瓶,加入10mL无水乙醇,常温磁力搅拌2小时,反应结束,减压蒸馏除去溶剂,然后用二氯甲烷萃取,减压蒸馏,得到黄色固体化合物,其核磁共振氢谱如图1,产率65%。1H-NMR(400MHz,DMSO-d6)δ(ppm):10.118(s,2H,-OH),7.616-7.523(m,7H,Ar-H),7.244-7.113(m,10H,Ar-H),6.908-6.894(d,J=5.6Hz,3H,Ar-H),6.849-6.824(t,2H,J=5Hz,Ar-CH=CH)。
实施例2
3,3'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯醇酸钾的合成
3,3'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯酚(1.00g,2.4mmol)、氢氧化钾(0.29g,5.3mmol)加入50mL单口烧瓶,加入10mL无水乙醇,常温磁力搅拌2小时,反应结束,减压蒸馏除去溶剂,然后用二氯甲烷萃取,减压蒸馏,得到黄色固体化合物,其核磁共振氢谱如图2,产率67%。1H-NMR(400MHz,DMSO-d6)δ(ppm):10.028(s,2H,-OH),7.616-7.523(m,7H,Ar-H),7.244-7.113(m,10H,Ar-H),6.908-6.894(d,J=5.6Hz,3H,Ar-H),6.849-6.824(t,2H,J=5Hz,Ar-CH=CH)。
实施例3
4,4'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯醇酸钾的合成
4,4'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯酚(1.00g,2.4mmol)、氢氧化钾(0.29g,5.3mmol)加入50mL单口烧瓶,加入10mL无水乙醇,常温磁力搅拌2小时,反应结束,减压蒸馏除去溶剂,然后用二氯甲烷萃取,减压蒸馏,得到黄色固体化合物,其核磁共振氢谱如图3,产率68%。1H-NMR(400MHz,DMSO-d6)δ(ppm):10.008(s,2H,-OH),7.616-7.523(m,7H,Ar-H),7.244-7.113(m,10H,Ar-H),6.908-6.894(d,J=5.6Hz,3H,Ar-H),6.849-6.824(t,2H,J=5Hz,Ar-CH=CH)。
实施例4
在温度为298K条件下,在质量比为3.5%的氯化钠溶液中对铜试样进行了失重实验,作为空白实验。选择失重实验的时间为30天,然后铜试样在蒸馏水、无水乙醇中超声清洗置于干燥器中干燥一天,最后称重测量。在相同的条件下,利用20g的铜样品做三组平行实验,求出平均失重为2.721g。
实施例5
在温度为298K条件下,在含2,2'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯醇酸钾缓蚀剂的质量比为3.5%的氯化钠溶液中对铜试样进行了失重实验。选择失重实验的时间为30天,缓蚀剂浓度为1.5mmol/L的条件下进行,然后铜试样在蒸馏水、无水乙醇中超声清洗置于干燥器中干燥一天,最后称重测量。在相同的条件下,利用20g的铜样品做三组平行实验,求出平均失重为0.115g。与空白试验对比,表明2,2'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯醇酸钾对铜具有良好的缓蚀作用。
实施例6
在温度为298K条件下,在含3,3'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯醇酸钾缓蚀剂的质量比为3.5%的氯化钠溶液中对铜试样进行了失重实验。选择失重实验的时间为30天,缓蚀剂浓度为1.5mmol/L的条件下进行,然后铜试样在蒸馏水、无水乙醇中超声清洗置于干燥器中干燥一天,最后称重测量。在相同的条件下,利用20g的铜样品做三组平行实验,求出平均失重为0.110g。与空白试验对比,表明3,3'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯醇酸钾对铜具有良好的缓蚀作用。
实施例7
在温度为298K条件下,在含4,4'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯醇酸钾缓蚀剂的质量比为3.5%的氯化钠溶液中对铜试样进行了失重实验。选择失重实验的时间为30天,缓蚀剂浓度为1.5mmol/L的条件下进行,然后铜试样在蒸馏水、无水乙醇中超声清洗置于干燥器中干燥一天,最后称重测量。在相同的条件下,利用20g的铜样品做三组平行实验,求出平均失重为0.104g。与空白试验对比,表明4,4'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯醇酸钾对铜具有良好的缓蚀作用。

Claims (3)

1.一类水溶性双希夫碱钾盐作为铜的缓蚀剂,其化学结构式如下:
其中结构式中C1,R1=-OK,R2=R3=H;C2,R2=-OK,R1=R3=H;C3,R3=-OK,R1=R2=H。
2.如权利要求1所述的缓蚀剂的合成方法,其特征步骤如下:
合成路线:
其中结构式(I)中C1,R1=-OK,R2=R3=H;C2,R2=-OK,R1=R3=H;C3,R3=-OK,R1=R2=H.
合成步骤:
将2,2'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯酚与氢氧化钾以摩尔比为1:2.2加入50mL单口烧瓶,加入体积为2,2'-(1E,1'E)-(4,4'-((E)-乙烯-1,2-二基)二(4,1-亚苯基))二(氮烷-1-基-1-亚基)二(甲烷-1-基-1-亚基)二苯酚8~10倍的无水乙醇,常温磁力搅拌2小时,反应结束,减压蒸馏除去溶剂,然后用二氯甲烷萃取,减压蒸馏,得到权利要求1的化合物。
3.如权利要求1所述的水溶性双希夫碱钾盐的缓蚀剂,其用途是:该缓蚀剂能够在质量比为3.5%的氯化钠溶液中保护铜金属不被腐蚀。
CN201610658625.6A 2016-08-11 2016-08-11 一类水溶性双希夫碱钾盐的合成与应用 Pending CN106278938A (zh)

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CN110627681A (zh) * 2018-12-21 2019-12-31 重庆师范大学 一种质子化亚胺分子及其金属铜缓蚀剂的合成方法

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CN110627681A (zh) * 2018-12-21 2019-12-31 重庆师范大学 一种质子化亚胺分子及其金属铜缓蚀剂的合成方法
CN110627681B (zh) * 2018-12-21 2022-06-17 重庆师范大学 一种质子化亚胺分子及其金属铜缓蚀剂的合成方法
CN110552008A (zh) * 2019-09-19 2019-12-10 桂林理工大学 2,6-吡啶二甲醛缩2-氨基芴希夫碱缓蚀剂的制备方法及其应用

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