3923-52-2Relevant articles and documents
Syntheses and characterizations of Zn (Ⅱ) Phthalocyanines & Naphthopyrans based polymers for improved nonlinear optical properties
Dong, Wenyue,Duan, Qian,Gao, Bo,Liu, Dajun,Wang, Jihua
, (2020)
In this paper, four organic polymers of poly [(MMA)x-co-(NPMA)y-co-(CPMA)z] and four zinc phthalocyanine (ZnPc) polymers of poly [(MMA)x-co-(NPMA)y-co-(ZnPc)z] have been successfully synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization, where MMA is methyl methacrylate, NPMA is 3,3-diphenyl-8-methacryloxy-3H-naphtho [2,1-b]pyran, and CPMA is 3,4-dicyanophenyl methacrylate. The components of these polymers have been fully characterized by 1H and 13C NMR, FT-IR, Raman, XPS, UV–Vis, and photoluminescence (PL) spectroscopy. From PL spectra, poly [(MMA)x-co-(NPMA)y-co-(ZnPc)z] polymers display strong fluorescence quenching by the energy transfer (ET) process between NPMA and ZnPc moieties. The third-order nonlinear optical (NLO) properties of poly [(MMA)x-co-(NPMA)y-co-(ZnPc)z] polymers have been investigated by the Z-scan technique, and poly [(MMA)168-co-(NPMA)5.2-co-(ZnPc)1.2] (Q4) showed the best NLO properties owing to the much stronger ET between NP and ZnPc units. Furthermore, it is essential to obtain doped poly (methyl methacrylate) (PMMA) films for practical application. The poly [(MMA)168-co-(NPMA)5.2-co-(ZnPc)1.2]/PMMA film exhibited a higher nonlinear absorption coefficient of 61 × 10?11 m/W and a lower limiting threshold of 0.19 J/cm2. The significantly enhanced NLO properties of poly [(MMA)168-co-(NPMA)5.2-co-(ZnPc)1.2]/PMMA film compared with solution are attributed to the weaker aggregation effect in PMMA film. This research provides a promising molecular design strategy for high performance NLO materials.
Fluorocyclization of Allyl Alcohols and Amines to Access 3-Functionalized Oxetanes and Azetidines
Cao, Shanshan,Li, Linxuan,Liu, Zhaohong,Ning, Yongquan,Wu, Yong,Zanoni, Giuseppe,Zhang, Qi,Zhang, Xinyu
supporting information, p. 3674 - 3679 (2021/05/31)
An efficient method to prepare 3-functionalized oxetanes and azetidines has been realized by fluorocyclization of readily available 2-azidoallyl/2-alkoxyallyl alcohols and amines. Notably, this is the first example applying the fluorocyclization strategy to construct four-membered heterocycles. The pendant electron-donating group (-N3 or -OR) plays a crucial role in polarizing the C= C double bond and facilitating the cyclization process, as verified by DFT and experimental studies.
Calcium-Catalyzed Intramolecular Hydroamination-Deacylation Reaction of in situ formed β-Amino Allenes
Yaragorla, Srinivasarao,Latha, Dandugula Sneha,Rajesh, Pallava
supporting information, p. 5486 - 5492 (2021/12/10)
We have developed a simple, One-Pot, three-component reaction of tert-propargyl alcohols, primary amines and acyl ketones to synthesize fully substituted pyrroles and pyridine derivatives in good to excellent yields with large substrate diversity. An eco-friendly calcium catalyst catalyzes the reaction to form the key intermediate β-amino allene that undergoes subsequent Thorpe-Ingold effect assisted hydroamination and aromaticity driven deacylation reaction to yield fully substituted five and six-membered azacyclic compounds. (Figure presented.).