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摘要:为有效对抗高、超光谱成像侦察威胁，实现迷彩绿色涂料与植物的"同谱同色"，本文基于酞菁与叶绿素卟啉结构的相似性，开展酞菁化合物合成及植物光谱特征拟合研究。构建吸电子取代基团和二价过渡族中心离子的平面酞菁结构，采用DBU催化法和自制合成装置合成酞菁化合物，探究最佳合成条件和提纯方法，采用分光光度计测试产物的吸收光谱和反射光谱，研究中心离子与聚集方式对酞菁化合物光谱性能的影响。实验结果表明，在催化剂作用下，四硝基金属酞菁在240~250℃时反应时间最短；钴酞菁比铁、锌、铜等作为中心取代离子形成的酞菁产物具有更尖锐的吸收峰，与绿色植物光谱曲线更相似；酞菁化合物的光谱反射曲线随温度、纯度及分散状态对产物聚集状态影响而产生移动。在220~240℃下合成20~30 min的四-硝基钴酞菁吸收光谱符合酞菁化合物Q带吸收特征，且其峰值波长与植物光谱相拟合，为酞菁类颜料在军事、纺织、染料、仿生等领域的应用提供了新方法和新途径。Abstract:In order to effectively resist the threat of hyperspectral imaging and reconnaissance and achieve "the same spectrum and color" of camouflage paint and plants, based on the similarity between phthalocyanine and chlorophyll porphyrin structure, the synthesis of phthalocyanine compounds and the fitting of plant spectral features are carried out. The planar phthalocyanine structure of the electron-withdrawing substituent and the divalent transition center ion is constructed. The phthalocyanine compounds are synthesized by DBU catalysis and self-made synthesis equipment. The optimal synthesis conditions and purification methods are investigated. The absorption and reflectance spectra of the products are tested by spectrophotometer to study the influence of central ion and aggregation on the spectral properties of phthalocyanine compounds. The experimental results show that the reaction time of tetranitrometal phthalocyanine is the shortest at 240~250℃ under the action of catalyst; cobalt phthalocyanine has a sharper absorption peak than the phthalocyanine product formed by iron, zinc, copper and other centrally substituted ions, which is more similar to the green plant spectral curve; the spectral reflection curve of the phthalocyanine compound shifts with the influence of temperature, purity and dispersion state on the product aggregation state. The absorption spectrum of tetra-nitro cobalt phthalocyanine synthesized at 220~240℃ for 20~30 min are in agreement with the Qband absorption characteristics of phthalocyanine compounds, and its peak wavelengths are matched with the plant spectrum. It provides new methods and new approaches for the application of phthalocyanine pigments in the fields of military, textile, dye and bionic etc.
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图 1金属酞菁DBU催化合成原理示意图
Figure 1.A schematic diagram of DBU catalytic synthesis of metal phthalocyanine
图 2自主设计合成装置及合成工艺示意图
(1.聚四氟乙烯磁子, 2.高温温度计, 3.冷凝管, 4.集热式磁力搅拌器, 5.甲基硅油油浴锅, 6.反应液)
Figure 2.Schematic diagram of self-designed synthesis device and synthetic process
(1.Teflon polyethylene magneton; 2.High temperature thermometer; 3.Condensing tube; 4.Heat magnetic mixer; 5.Methyl silicone oil bath wok; 6.Reaction liquid)
图 4不同中心金属的反应时间与反应温度
Figure 4.Reaction time and reaction temperature of different central metals
图 6酞菁吸收峰曲线(上)与光谱反射曲线(下)
Figure 6.Phthalocyanine absorption peak curve(top) and spectral reflection curve(below)
图 7不同纯度四硝基酞菁铁的光谱反射曲线
Figure 7.Spectral reflectance curves of different purity tetral phthalocyanine iron metals
图 8不同纯度四硝基酞菁钴的光谱反射曲线
Figure 8.Spectral reflectance curves of different purity tetra-nitrophthalocyanine cobalt metals
图 10不同浓度、湿度的样品反射光谱曲线
Figure 10.Sample reflectance spectra of different concentrations and humidity
图 11不同温度分散的样品反射光谱曲线
Figure 11.Sample reflectance spectra of different temperature dispersion
表 1原料剂表
Table 1.Ingredient list
名称 规格 试剂厂家 N, N-二甲基乙酰胺 AR 科龙化工 二氯甲烷 AR Tansoole DBU 99% 阿拉丁 乙醇 AR 南京化学试剂厂 甲醇 AR 西陇化工 各种金属氯化物 AR 西陇化工 4-硝基邻苯二甲腈 98% 阿拉丁 石英砂 60~80目AR 南京化学试剂厂 硅胶 200目AR 南京化学试剂厂 
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表 2金属酞菁最佳合成条件
Table 2.Optimum synthesis conditions of metal phthalocyanine
产物 反应温度/℃ 反应时间/min 表观颜色 四硝基酞菁铁(TNFePC) 270±5 50±3 墨绿色 四硝基酞菁铬(TNCrPC) 230±5 30±3 深靛色 四硝基酞菁钴(TNCoPC) 230±5 30±3 深绿色 四硝基酞菁镍(TNNiPC) 220±5 20±3 深青色 四硝基酞菁铜(TNCuPC) 240±5 30±3 深蓝色 四硝基酞菁锌(TNZnPC) 220±5 20±3 青绿色 下载:
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