Two series monot ailed porphyrins, Cobalt-5- {4- [ω- （1-adamant aneamino） alkyloxy] phenyl }- 10,15,20-triphenyl porphyrinate （CoPCnA, n=4,5,6） and Nickel-5-{4-[ω-（1-adamantaneamino）alkyloxy]phenyl}-10,15.20- ...Two series monot ailed porphyrins, Cobalt-5- {4- [ω- （1-adamant aneamino） alkyloxy] phenyl }- 10,15,20-triphenyl porphyrinate （CoPCnA, n=4,5,6） and Nickel-5-{4-[ω-（1-adamantaneamino）alkyloxy]phenyl}-10,15.20- triphenyl porphyrinate （NiPCnA, n=4,5,6）, were synthesized, in which the porphyrin moiety was connected to l-adamantanamine via a flexible hydrocarbon chain. The fluorescence quenching between these donor substrates and mono-6-p-nitrobenzoyl-β-cyclodextrin （NBCD） was studied in detail. Distinct fluorescence quenching occured in these supramolecular systems. This quenching was attributed to the photoinduced electron transfer （PET） inside the supramolecular assembly between the porphyrin donors and cyclodextrin acceptors. Detailed Stern-Volmer constants were measured and they were partitioned into dynamic Stern- Volmer quenching constants and static binding constants. It was demonstrated that the PET interaction between the porphyrin subunits and NBCD is indeed effective.展开更多
1,3-Dipolar cycloaddition of DTE-azomethine ylides （DTE： dithienyl-ethene） to C60 in refluxed toluene was used to synthesize novel dumbbell-type fullerene dimer 1. For the sake of comparison, the monoadduct 2 were ...1,3-Dipolar cycloaddition of DTE-azomethine ylides （DTE： dithienyl-ethene） to C60 in refluxed toluene was used to synthesize novel dumbbell-type fullerene dimer 1. For the sake of comparison, the monoadduct 2 were also synthesized. The molecular geometries of these two compounds were determined by theoretical calculations with HF-3/21G method. UV-Vis and fluorescence experiments were carried out in solvents with different polarity at the room temperature. All the results indicated the existence of a photoinduced intramolecular electron transfer process between the donor and acceptor moieties.展开更多
Co-based metal-organic framework(MOF),a kind of porous crystal material composed of Co ions and organic linkers,is a common type of MOF.It not only has the intrinsic properties of MOF,such as structural diversity,func...Co-based metal-organic framework(MOF),a kind of porous crystal material composed of Co ions and organic linkers,is a common type of MOF.It not only has the intrinsic properties of MOF,such as structural diversity,functional adjustability,and high surface area,but more importantly,it contains Co metal species,which are considered by many reports to be active catalytic centers for many reactions.Meanwhile,metal catalysts always received wide and sustained attention.The combi-nation of the two types of catalysts can enhance the catalytic performance and achieve the"1+1>2"effect.In this review,we mainly overview the synthesis methods of Co-based MOF-derived metal catalysts from nano-to atom-level and their applications in the catalysis field in recent years and put forward our own views and prospects for this research direction.展开更多
We develop a novel coumarin-all〈yne derivative （NC7-AL）, which can specifically react with Au^3＋ and give a colorimetric and fluorescent ＂turn-on＂ response toward Au3~, Notably, other alkynophilic metal species ...We develop a novel coumarin-all〈yne derivative （NC7-AL）, which can specifically react with Au^3＋ and give a colorimetric and fluorescent ＂turn-on＂ response toward Au3~, Notably, other alkynophilic metal species such as Au^＋, Ag^＋, Pd^2＋, Ni^2＋, Cu^2＋, and Hg^2＋ do not produce an interfering signal. A good linear relationship between emission intensity at 420 nm and Au^3＋ concentration from 0 to 2 equivalent is observed, and the detection limit （3σ/k） is estimated to be ca. 3.58 nmol/L. Harnessing the Au^3＋ .展开更多
基金V. ACKN0WLEDGMENT This work was supported Science Foundation of China by the National Natural （No.20472079）.
文摘Two series monot ailed porphyrins, Cobalt-5- {4- [ω- （1-adamant aneamino） alkyloxy] phenyl }- 10,15,20-triphenyl porphyrinate （CoPCnA, n=4,5,6） and Nickel-5-{4-[ω-（1-adamantaneamino）alkyloxy]phenyl}-10,15.20- triphenyl porphyrinate （NiPCnA, n=4,5,6）, were synthesized, in which the porphyrin moiety was connected to l-adamantanamine via a flexible hydrocarbon chain. The fluorescence quenching between these donor substrates and mono-6-p-nitrobenzoyl-β-cyclodextrin （NBCD） was studied in detail. Distinct fluorescence quenching occured in these supramolecular systems. This quenching was attributed to the photoinduced electron transfer （PET） inside the supramolecular assembly between the porphyrin donors and cyclodextrin acceptors. Detailed Stern-Volmer constants were measured and they were partitioned into dynamic Stern- Volmer quenching constants and static binding constants. It was demonstrated that the PET interaction between the porphyrin subunits and NBCD is indeed effective.
基金Ⅴ. ACKN0WLEDGMENTS This work was supported by the National Natural Science Foundation of China （No.20332020 and No.20472079）.
文摘1,3-Dipolar cycloaddition of DTE-azomethine ylides （DTE： dithienyl-ethene） to C60 in refluxed toluene was used to synthesize novel dumbbell-type fullerene dimer 1. For the sake of comparison, the monoadduct 2 were also synthesized. The molecular geometries of these two compounds were determined by theoretical calculations with HF-3/21G method. UV-Vis and fluorescence experiments were carried out in solvents with different polarity at the room temperature. All the results indicated the existence of a photoinduced intramolecular electron transfer process between the donor and acceptor moieties.
基金The authors gratefully acknowledge the financial support from the Natural Science research project of Universities in Anhui Province(KJ2021ZD0001)the Natural Science Foundation of AnhuiProvince(2208085MB20).
文摘Co-based metal-organic framework(MOF),a kind of porous crystal material composed of Co ions and organic linkers,is a common type of MOF.It not only has the intrinsic properties of MOF,such as structural diversity,functional adjustability,and high surface area,but more importantly,it contains Co metal species,which are considered by many reports to be active catalytic centers for many reactions.Meanwhile,metal catalysts always received wide and sustained attention.The combi-nation of the two types of catalysts can enhance the catalytic performance and achieve the"1+1>2"effect.In this review,we mainly overview the synthesis methods of Co-based MOF-derived metal catalysts from nano-to atom-level and their applications in the catalysis field in recent years and put forward our own views and prospects for this research direction.
基金supported by the National Natural Science Foundation of China (Nos. 21102001, 21271035 and 21372005)Anhui Provincial Natural Science Foundation (No. 1608085MB39)+1 种基金Natural Science Foundation of Education Department of Anhui Province (Nos. KJ2015A047, KJ2014A013)211 Project of Anhui University
文摘We develop a novel coumarin-all〈yne derivative （NC7-AL）, which can specifically react with Au^3＋ and give a colorimetric and fluorescent ＂turn-on＂ response toward Au3~, Notably, other alkynophilic metal species such as Au^＋, Ag^＋, Pd^2＋, Ni^2＋, Cu^2＋, and Hg^2＋ do not produce an interfering signal. A good linear relationship between emission intensity at 420 nm and Au^3＋ concentration from 0 to 2 equivalent is observed, and the detection limit （3σ/k） is estimated to be ca. 3.58 nmol/L. Harnessing the Au^3＋ .
