Synthesis of a dendrimeric phenoxy-substituted cyclotetraphosphazene and its non-covalent interactions with multiwalled carbon nanotubes
摘要:
A dendrimeric phenoxy-substituted cyclotetraphosphazene has been prepared for the non-covalent functionalization of multiwalled carbon nanotubes (MWCNTs). The synthesized cyclotetraphosphazene derivatives (2-4) and dendrimeric cyclotetraphosphazene (5) have been characterized by standard spectroscopic techniques. The functionalization of MWCNTs with compound 5 has been accomplished and the resulting MWCNT-5 hybrid has been characterized by P-31 NMR, H-1 NMR, Raman spectroscopy, X-ray diffraction (XRD), energy dispersive X-ray (EDX), fluorescence, thermal gravimetric analysis (TGA) and high-resolution transmission electron microscopy (HRTEM) techniques. The results showed that the dendrimeric compound 5 has been attached to the MWCNTs via non-covalent "pi-pi" interactions between the phenoxy groups on the dendrimeric compound 5 and the extended it system of the MWCNTs. The MWCNT-5 hybrid exhibited significant dispersion stability in common organic solvents. (C) 2013 Elsevier Ltd. All rights reserved.
Structural and chemosensor properties of FDA and FDP derivatives of fluorenylidene bridged cyclotetraphosphazenes
作者:Elif Şenkuytu、Gönül Yenilmez Çiftçi
DOI:10.1016/j.poly.2016.04.046
日期:2016.9
The first series of 4,4'-(9-fluorenylidene)diphenol (FDP) (5) and 4,4'-(9-fluorenylidene)dianiline (FDA) (6) bridged and open chained cyclotetraphosphazene derivatives (15-23) have been synthesized. Their florescence and chemosensor properties are reported. Nucleophilic substitution reactions of octachlorocyclotetraphosphazene (1) with mono-functional reagents [phenol (2), 2-naphthol (3) and 1-hydroxypyrene (4)] were carried out and the heptasubstituted derivatives (8, 11 and 14) were obtained. Then the reactions of 8, 11 and 14 with 4,4'-(9-fluorenylidene)diphenol (FDP) (5) and 4,4'-(9-fluorenylidene)dianiline (FDA) (6), respectively gave bridged and open chained compounds. The structures of the synthesized compounds (7-23) were verified by elemental analyses, mass spectrometry, DV Vis, H-1 and P-31 NMR techniques and fluorescence spectroscopy. The metal sensing properties of the novel bridged open chain cyclotetraphosphazene derivatives were also examined by fluorescence spectroscopy. These complexes showed high selectivity for Cu2+ and Fe3+ ions in solution. (C) 2016 Elsevier Ltd. All rights reserved.
US7317046B2
申请人:——
公开号:US7317046B2
公开(公告)日:2008-01-08
Synthesis of a dendrimeric phenoxy-substituted cyclotetraphosphazene and its non-covalent interactions with multiwalled carbon nanotubes
作者:Elif Okutan、Bünyemin Çoşut、Saadet Beyaz Kayıran、Mahmut Durmuş、Adem Kılıç、Serkan Yeşilot
DOI:10.1016/j.poly.2013.09.011
日期:2014.1
A dendrimeric phenoxy-substituted cyclotetraphosphazene has been prepared for the non-covalent functionalization of multiwalled carbon nanotubes (MWCNTs). The synthesized cyclotetraphosphazene derivatives (2-4) and dendrimeric cyclotetraphosphazene (5) have been characterized by standard spectroscopic techniques. The functionalization of MWCNTs with compound 5 has been accomplished and the resulting MWCNT-5 hybrid has been characterized by P-31 NMR, H-1 NMR, Raman spectroscopy, X-ray diffraction (XRD), energy dispersive X-ray (EDX), fluorescence, thermal gravimetric analysis (TGA) and high-resolution transmission electron microscopy (HRTEM) techniques. The results showed that the dendrimeric compound 5 has been attached to the MWCNTs via non-covalent "pi-pi" interactions between the phenoxy groups on the dendrimeric compound 5 and the extended it system of the MWCNTs. The MWCNT-5 hybrid exhibited significant dispersion stability in common organic solvents. (C) 2013 Elsevier Ltd. All rights reserved.
Synthesis, optical, and structural properties of bisphenol-bridged aromatic cyclic phosphazenes
作者:Bünyemin ÇOŞUT、Burcu TOPALOĞLU AKSOY、Süreyya Oğuz TÜMAY、Ahmet ŞENOCAK、Serkan YEŞİLOT
DOI:10.3906/kim-1907-73
日期:——
Phenoxy- and naphthoxy-substituted bisphenol-bridged cyclicphosphazenes were synthesized in 2 steps and their thermal, photophysical, and electrochemical properties were investigated. The structures of the cyclicphosphazene compounds were determined by ESI-MS mass spectrometry and 1 H, 13 C, and 31 P NMR spectroscopies. The photophysical studies of phenoxy- and naphthoxy-substituted bridged cyclophosphazenes
分两步合成了苯氧基和萘氧基取代的双酚桥联环状磷腈,并研究了它们的热、光物理和电化学性能。环状磷腈化合物的结构通过ESI-MS质谱法和1 H、 13 C和31 P NMR光谱测定。通过不同溶剂中的吸收光谱和荧光光谱研究了苯氧基和萘氧基取代的桥联环磷腈的光物理研究。还研究了目标化合物的热性能和电化学性能。此外,通过荧光光谱研究了溶液和固态中分子内相互作用引起的准分子发射,并使用DFT进行了详细的理论计算。