Development of a novel Cd(ii) metal complex for solvent-sensitive detection of Zn(ii) and Mg(ii) with the formation of Cd(ii)–Zn(ii)/Cd(ii)–Mg(ii) complexes and their application in effective Schottky devices
文献情報
Dibyendu Sathapat, Mainak Das, Manik Das, Uttam Kumar Das, Arijit Bag, Soumik Laha, Partha Pratim Ray, Bidhan Chandra Samanta, Tithi Maity
The novel mononuclear Cd(II) metalloreceptor Cd[LH2I2] (complex 1), derived by the reaction of the Schiff base ligand 6,6′-(1E,1′E)(ethane-1,2 diylbis(azaneylidene))bis(methaneylylidene)bis(2-ethoxyphenol) (H2L) and CdI2, was successfully used to detect Zn(II) and Mg(II) in semi-aqueous and aqueous media, respectively, among several competitive cations. The single crystal data analysis revealed that the asymmetric unit of complex 1 consists of one ligand, H2L, and two I-ions, compensating the +2 oxidation state of Cd. The optically monitored sensing of Zn(II) and Mg(II) by complex 1 was further assessed by utilizing UV and fluorescence spectroscopic techniques. The remarkable enhancement of the fluorescence intensity of complex 1-Zn(II) and complex 1-Mg(II) in the presence of CH3COO− and SO4= indicated that a heteronuclear bridging complex could be obtained if two separate reactions of complex 1 with (CH3COO)2Zn and MgSO4 could be carried out. Interestingly, two different single crystals of Cd–Zn (complex 2) and Cd–Mg (complex 3) were obtained after conducting two separate reactions of complex 1 with Zn(II) and Mg(II). Single crystal data analysis showed that complex 2 is an octanuclear Zn(II)/Cd(II) complex with the presence of acetate and an hydroxy group, and both metal centers are in the +2 oxidation state. The IR and NMR spectra results confirmed the formation of complexes 2 and 3. The SPX and EDX studies confirmed the presence of Zn(II) and Mg(II) in complex 2 and complex 3, respectively. The limit of detection for sensing of both was measured in the nanomolar range. Although it is well-known that mononuclear Cd complexes are effective Schottky devices, there have been few reports of investigation of heteronuclear Cd(II) complexes as candidates for effective Schottky devices, or determination of the values of device performance, conductivity, and device parameters with heteronuclear Cd complexes 2 and 3. Surprisingly, all the results indicated that a potential Schottky device could be produced due to the efficacy of complex 2 with respect to complex 3. The effectiveness of the device would be satisfactory because of the lower band gap value and the presence of weak intramolecular π–π stacking interactions in complex 2.
関連文献
Affinity-based precipitation via a bivalent peptidic hapten for the purification of monoclonal antibodies
Michael W. Handlogten, Jared F. Stefanick, Peter E. Deak
DOI: 10.1039/C4AN00780H
Novel DFO-SAM on mesoporous silica for iron sensing. Part I. Synthesis optimization and characterization of the material
Raffaela Biesuz, Giovanni Emma, Chiara Milanese, Giacomo Dacarro, Angelo Taglietti, Valeria Marina Nurchi, Giancarla Alberti
DOI: 10.1039/C4AN00179F
Dip-pen microarraying of molecular beacon probes on microgel thin-film substrates
Xiaoguang Dai, Matthew Libera
DOI: 10.1039/C4AN01220H
Aptamer-based competitive binding assay for one-step quantitation of hepatitis B surface antigen
Sung-Kwan Suh, Seongeun Song, Heung-Bum Oh, Sang Soo Hah
DOI: 10.1039/C4AN00619D
Webcam-based flow cytometer using wide-field imaging for low cell number detection at high throughput
Hugh Alan Bruck
DOI: 10.1039/C4AN00669K
Methane–oxygen electrochemical coupling in an ionic liquid: a robust sensor for simultaneous quantification
Zhe Wang, Min Guo, Gary A. Baker, Joseph R. Stetter, Lu Lin, Andrew J. Mason, Xiangqun Zeng
DOI: 10.1039/C4AN00839A
A sensitive dual colorimetric and fluorescence system for assaying the activity of alkaline phosphatase that relies on pyrophosphate inhibition of the peroxidase activity of copper ions
Ki Soo Park, Chang Yeol Lee, Hyun Gyu Park
DOI: 10.1039/C4AN00778F
Plasmonic nanoparticle-film calipers for rapid and ultrasensitive dimensional and refractometric detection
Chen-Chieh Yu, Keng-Te Lin, Yi-Chuan Tseng, Sin-Yi Chou, Chang-Ching Shao, Hsuen-Li Chen, Wei-Fang Su
DOI: 10.1039/C4AN00186A
こちらもおすすめ
3-(5-フェニル-2-ファイル)-プロパン酸の市場動向や研究トレンドはどうですか?
この化合物の市場動向は不明ですが、類似化合物の需要は化学繊維、医薬品、農薬分野で安定しています。研究トレンドとしては、該当化合物の生物学的活性の評価や、その他の...
3- Chloro-1H-indazol-5-olはどのように保存すればよいですか?
3- チロロ-1H-吲唑-5-醇は遮光し、直射日光を避けて、温度は室温を推奨し、密閉容器に保存してください。
L-(1-~13~C)メチオニンの市場動向や研究トレンドはどうですか?
L-(1-~13~C)メチオニンは、医薬品やバイオテクノロジー分野での研究が増加しており、その価格は安定しています。新興研究分野では、代謝解析や遺伝子機能解析で...
1,3-フェニレンビスメチレンビスアクリレートは安全ですか?
1,3-フェニレンビスメチレンビスアクリレートは一般的に安全ですが、直接皮膚に触れる場合は保護用具を使用することを推奨します。高濃度の蒸気が吸入された場合は呼吸...
丹参醇Aはどのように保存すればよいですか?
丹参醇Aは、直射日光を避けて室温で保存し、密栓容器に入れることをお勧めします。適切な保存条件は、安定性を保ち、安全性を確保する上で重要です。
4-メチル-2-(1,1,1-三フロロ-2-メチルプロパニル)ピリドインとは何ですか?
CAS番号1378865-93-0の4-メチル-2-(1,1,1-三フロロ-2-メチルプロパニル)ピリドインは、合成化学分野で用いられる有機化合物の一種です。こ...
N-フェニルベンジル-2-クロロ酢氨を取り扱う際の実験室安全事項は何ですか?
N-フェニルベンジル-2-クロロ酢氨は毒性があり、皮膚や粘膜に刺激を与えます。取り扱う際には、保護眼鏡、手袋、ゴーグルを着用することを強く推奨します。ドラフトチ...
UCN-02を取り扱う際の実験室安全事項は何ですか?
UCN-02は毒性は低いですが、人体への直接的な接触は避けるべきです。PPE要件はグローブと顔面保護具を着用することです。ドラフトチャンバーを使用して漏洩を処理...
N-[3-[2-(二甲基氨基)乙氧基]-4-甲氧基苯基]-2'-甲基-4'-(5-甲基-1,2,4-恶二唑-3-基)-[1,1'-联苯]-4-甲酰胺を取り扱う際の実験室安全事項は何ですか?
手袋と保護眼鏡を着用し、漏洩時には吸気防止装置を使用してください。室温、乾燥した場所に保管し、直日光から隔離してください。SDS(安全データシート)を参照してく...
掲載誌
New Journal of Chemistry

NJC (New Journal of Chemistry) is a broad-based primary journal encompassing all branches of chemistry and its sub-disciplines. It contains full research articles, communications, perspectives and focus articles. This well-established journal, owned by the Centre National de la Recherche Scientifique (CNRS) of France, has been co-published with the Royal Society of Chemistry since January 1998. NJC is the forum for the publication of high-quality, original and significant work that opens new directions in chemistry or other scientific disciplines. In addition to having a significant chemical component, work published in NJC must demonstrate that it will have an impact on areas of research other than that of the reported work.













![2,9-Dichloro-5,12-dihydroquinolino[2,3-b]acridine-7,14-dione structure 2,9-Dichloro-5,12-dihydroquinolino[2,3-b]acridine-7,14-dione structure](https://static.chemtradehub.com/structs/308/3089-17-6-750b.webp)
![2,2'-{2,2-Propanediylbis[(2,6-dibromo-4,1-phenylene)oxy]}diethanol structure 2,2'-{2,2-Propanediylbis[(2,6-dibromo-4,1-phenylene)oxy]}diethanol structure](https://static.chemtradehub.com/structs/416/4162-45-2-b3d6.webp)