Six glucoside compounds have been synthesized by means of phase-transfer catalytic method and deacetylation from the starting material ferrocene. Their structures have been confirmed by elementary analysis, IR,1HNMR a...Six glucoside compounds have been synthesized by means of phase-transfer catalytic method and deacetylation from the starting material ferrocene. Their structures have been confirmed by elementary analysis, IR,1HNMR and MS. The antianemic activities of some compounds have also been tested. Results indicate that these glucoside compounds possess the antianemic activities and therefore, the further study is well worth making.展开更多
A series of new stable (thermal and photochemical) ferrocenyl derivatives containing C=N bond and benzene ring in long conjugated chains have been synthesized and characterized by (HNMR)-H-1(400MHz), IR, and elemental...A series of new stable (thermal and photochemical) ferrocenyl derivatives containing C=N bond and benzene ring in long conjugated chains have been synthesized and characterized by (HNMR)-H-1(400MHz), IR, and elemental analysis. Pull-push ferrocenyl complexes that we have prepared have strong NLO responses identified by electronic absorption spectrum.展开更多
Ferrocenyliminophosphine 1 and 1,1′-bisferrocenyliminophosphine 2 were easily prepared from the condensation of formylferrocene or 1,1′-diformylferrocene with 2-（diphenylphosphino） aniline. The following reduction...Ferrocenyliminophosphine 1 and 1,1′-bisferrocenyliminophosphine 2 were easily prepared from the condensation of formylferrocene or 1,1′-diformylferrocene with 2-（diphenylphosphino） aniline. The following reduction of imine group by LiAlH4 led to the formation of the corresponding ferrocenyl amidophosphines 3 and 4. The new ligands 2- 4 were well characterized by IR, ^1H NMR, ^31p NMR spectra, elemental analysis, and ESI-MS. The catalytic activity of all the ligands with palladium compounds in the Suzuki reaction was evaluated. Ligand 1, in combination with Pd （OAc）2, was found to be the most effective for the Suzuki reaction of aryl bromides with phenylboronic acid. Typically, the use of 0. 1% （molar fraction） of Pd（OAc）2/ligand 1 in the presence of two equivalents of K2CO3 as base in toluene at 110 ℃ provided good to excellent yields of the coupled products.展开更多
A new approach to fullerene ferrocenyl derivative has been made. [60]Fullerene reacts with ferrocenylmethyl azide to give N-ferrocenylmethyl imino[60]fullerene in 42% yield.
Reaction of Zn（NO3）2·6H2O with 3-（4-carboxylphenylamino）-l-ferrocenyl-2-butylen-l-one （HL） and 4,4′-bipyfidine （4,4′- bipy） in methanol solution resulted in a novel ladder-like coordination polymer {[Zn...Reaction of Zn（NO3）2·6H2O with 3-（4-carboxylphenylamino）-l-ferrocenyl-2-butylen-l-one （HL） and 4,4′-bipyfidine （4,4′- bipy） in methanol solution resulted in a novel ladder-like coordination polymer {[Zn2L2（μ2-L）2（4,4′-bipy）2]·MeOH}n （1）. Its crystal structure, thermal and electrochemical properties are presented.展开更多
Novel ferrocenyl derivatives of p-(10-mercaptodecyloxy) benzal 4-ferrocenylaniline have been prepared and characterized by element analysis, 1HNMR, and FAB-MS. Cyclic voltammetry has been used to characterize the self...Novel ferrocenyl derivatives of p-(10-mercaptodecyloxy) benzal 4-ferrocenylaniline have been prepared and characterized by element analysis, 1HNMR, and FAB-MS. Cyclic voltammetry has been used to characterize the self-assembled monolayers formed from the compounds on the gold electrodes.展开更多
The single crystal structure of the donor-acceptor ferrocenyl derivativeC18H15ClFe (Mr = 322. 62 ) has been determined, belonging to orthorhombic crystalsystem, space group P212121 with lattice parameters a= 11. 307 (...The single crystal structure of the donor-acceptor ferrocenyl derivativeC18H15ClFe (Mr = 322. 62 ) has been determined, belonging to orthorhombic crystalsystem, space group P212121 with lattice parameters a= 11. 307 (2), b= 8. 471 (2 ), c=15. 427(3) A, V= 1477. 7(9) A3, Z=4, D.= 1. 45 g. cm-3, λ(MoKα) =0. 71073A,μ= 11. 9 cm-1, F(000) = 664. The final R value for 1534 observed [I>3σ(I)] reflec-tions is 0. 060. The configuration of the C =C double bond is trans. The C5H4CH =CHC6H4Cl fragrnent is almost planar. The rings of ferrocene are almost in the eclipsedpositions with each other.展开更多
Redox-active polyelectrolyte-surfactant complexes（PSC） were prepared via the ionic self-assembly of sodium poly（styrenesulfonate） （PSS） and ferrocenyl surfactant,（11-ferrocenylundecyl）trimethylammonium bromide...Redox-active polyelectrolyte-surfactant complexes（PSC） were prepared via the ionic self-assembly of sodium poly（styrenesulfonate） （PSS） and ferrocenyl surfactant,（11-ferrocenylundecyl）trimethylammonium bromide（FTMA） in aqueous solution. The PSS-FTMA complex exhibited an ordered interdigitated monolayer mesomorphous structure with the long period of d = 3.13 nm,and was in the ionic thermotropic liquid crystal SmA state at room temperature.Interestingly,in the solid complex, the ferrocenyl moieties formed H-aggregation showing an increase in theπ-π~＊ energy transfer of cyclopentadienes in the ferrocene moieties as known from the blue-shift in the UV spectrum.The complexes showed higher thermal stability compared with their components due to the ionic interaction.The PSS-FTMA film had a good redox reversibility,which promised to be used in electrochemical sensors.展开更多
Two new [60]fullerene ferrocenylmethyl derivatives have been prepared via different approaches and characterized by UV-Vis, FT-IR, NMR, FAB-MS spectra and VPO. The second approach, i.e reacting fullerene with ferrocen...Two new [60]fullerene ferrocenylmethyl derivatives have been prepared via different approaches and characterized by UV-Vis, FT-IR, NMR, FAB-MS spectra and VPO. The second approach, i.e reacting fullerene with ferrocenylmethyl azide directly, was never reported as yet.展开更多
A novel chiral bis(ferrocenyl) P2N ligand 1 with C2-symmetry was synthesized through a four-step procedure from (R)-N,N-dimethyl-1-ferrocenylethylamine. In a model reaction of Pd-catalyzed allylic alkylation of 1,3-d...A novel chiral bis(ferrocenyl) P2N ligand 1 with C2-symmetry was synthesized through a four-step procedure from (R)-N,N-dimethyl-1-ferrocenylethylamine. In a model reaction of Pd-catalyzed allylic alkylation of 1,3-diphenylprop-2-enyl acetate 6 with dimethyl malonate, good enantioselectivity (86% e.e.) was obtained.展开更多
A new type of ferrocenyl thia crown ethers used as selective ligands to some poisonous metals was synthesized, and the features of their mass spectra in electron ionization mode were summarized as: (1) the strong mol...A new type of ferrocenyl thia crown ethers used as selective ligands to some poisonous metals was synthesized, and the features of their mass spectra in electron ionization mode were summarized as: (1) the strong molecular ion peaks; (2) a characteristic homologous ion series with sequential loss of C 2H 4S or C 2H 4O from M C 5H 5; (3) a new rearrangement reaction of Fe migration; (4) the uncommon loss of alcohol or thiol from the fragments of Fe rearrangement. Some typical fragmentation patterns were discussed in detail with the aid of exact mass measurement and MS/MS technique.展开更多
Much interest has been devoted to organometallic NLO materials. We have become interested in exploring the utility of ferrocenyl group as the conjugating bridge. Thus, we synthesized 1-{{[1,3-(5-methylbenzo)dithiol]-2...Much interest has been devoted to organometallic NLO materials. We have become interested in exploring the utility of ferrocenyl group as the conjugating bridge. Thus, we synthesized 1-{{[1,3-(5-methylbenzo)dithiol]-2-yli- dene}methyl}-1’-[2-(p-nitrophenyl)-(E)-ethenyl]ferrocene (1). This new ferrocenyl compound has a donor and an acceptor group in 1,1’-positions. Investigations of the solvatochromic property of the compound revealed that it has polarized structure in a polar solvent, such as DMF. SHG efficiency of the compound was estimated by an SHEW (second-harmonic generation with the evanescent wave) method.展开更多
The title complex [Fc（OCH3）PS2Ir（cod）] （1, Fc = Fe（η^5-C5H4）（η^5-C5H5）, cod = 1,5-cyclooctadiene） has been prepared and characterized by X-ray diffraction analysis. It crystallizes in monoclinic, space gro...The title complex [Fc（OCH3）PS2Ir（cod）] （1, Fc = Fe（η^5-C5H4）（η^5-C5H5）, cod = 1,5-cyclooctadiene） has been prepared and characterized by X-ray diffraction analysis. It crystallizes in monoclinic, space group P21/n with a = 12.5567（5）, b = 13.5197（5）, c = 11.7833（4） A, β = 99.651（2）°, V = 1972.06（13）A^3, Z = 4, Mr = 611.52, Dc = 2.06 g/cm^3, μ（MoKα） = 7.775 mm^-, F（000） = 1184, S = 1.063, the final R = 0.0199 and wR = 0.0468 for 4063 observed reflections with I 〉 2σ（I） and 227 variables. The molecular structure of 1 shows that the central iridium atom is chelated by the [Fc（OCH3）PS2]-ligand via two sulfur atoms and coordinated by one η^4-cod molecule via four carbon atoms in a distorted octahedral coordination geometry. The average Ir-S and Ir-C bond lengths are 2.3712（8） and 2.122（3） A, respectively.展开更多
The reduction reagents prepared from sodium borohydride, I-2 and a catalytic amount of chiral ferrocenyl amino alcohols 2a-e have been successfully applied to the enantioselective reduction of ketones. The optically a...The reduction reagents prepared from sodium borohydride, I-2 and a catalytic amount of chiral ferrocenyl amino alcohols 2a-e have been successfully applied to the enantioselective reduction of ketones. The optically active secondary alcohols were obtained in moderate enantiomeric excess and high chemical yield.展开更多
Sodium 3-ferrocenyl-5-phenyl-pyrazoline-1-dithiocarbamate (FPPD) reacts with anhydrous rare earth chlorides in absolute ethanol to give 14 new complexes.The results of elemental analysis show that the compositions of ...Sodium 3-ferrocenyl-5-phenyl-pyrazoline-1-dithiocarbamate (FPPD) reacts with anhydrous rare earth chlorides in absolute ethanol to give 14 new complexes.The results of elemental analysis show that the compositions of the complexes are RE(FPPD)_3·nH_2O(RE=La,Pr～Lu and Y;n=3).The ligand and its complexes have been characterized by infrared spectroscopy,UV-visible absorption spectroscopy,~1H-NMR spectra,thermal analysis and molar conductivity measurement.展开更多
The oxygen evolution reaction(OER)is a key process in water splitting for hydrogen production,yet its sluggish kinetics pose significant challenges for catalyst development.In this work,we present the first systematic...The oxygen evolution reaction(OER)is a key process in water splitting for hydrogen production,yet its sluggish kinetics pose significant challenges for catalyst development.In this work,we present the first systematic study on isostructural 2D coordination polymers(CPs)based on 1,10-ferrocenediyl-bis(H-phosphinic)acid,with cobalt,manganese,and cadmium metals as electrocatalysts for OER.These polymers were synthesized via a facile solution reaction,yielding crystalline materials with excellent structural integrity.The electrocatalytic performance of CPs composites,prepared with carbon and phosphonium ionic liquid,was evaluated in 0.1 M KOH using a three-electrode system.Notably,the Co-and Cd-based CPs demonstrated exceptional OER activity,achieving an overpotential as low as 236–255 mV at 10 mA cm^(-2),surpassing those of many previously reported CP-based OER catalysts.Furthermore,these materials exhibited high stability over prolonged electrolysis,maintaining their activity without significant degradation.This work not only introduces a new class of ferrocenyl phosphinatebased CPs as highly active and durable OER catalysts but also provides valuable insights into their structureactivity relationships,paving the way for future advancements in electrocatalysis.展开更多
Optically active aziridino alcohols containing ferrocenyl groups were prepared from commercially available L-threonine in excellent yields and used as catalysts to promote the asymmetric addition of diethylzinc to ary...Optically active aziridino alcohols containing ferrocenyl groups were prepared from commercially available L-threonine in excellent yields and used as catalysts to promote the asymmetric addition of diethylzinc to aryalde-hydes to afford 1-arylpropanol in up to 84% enantiomeric excesses with moderate to good yields.展开更多
The asymmetric reduction of prochiral ketones was catalyzed by a class of recoverable and highly stable chiral ferrocenyl amino alcohols derived from natural amino acids to yield optically active secondary alcohols in...The asymmetric reduction of prochiral ketones was catalyzed by a class of recoverable and highly stable chiral ferrocenyl amino alcohols derived from natural amino acids to yield optically active secondary alcohols in high chemical yields and moderate to good enantiomeric excesses.展开更多
文摘Six glucoside compounds have been synthesized by means of phase-transfer catalytic method and deacetylation from the starting material ferrocene. Their structures have been confirmed by elementary analysis, IR,1HNMR and MS. The antianemic activities of some compounds have also been tested. Results indicate that these glucoside compounds possess the antianemic activities and therefore, the further study is well worth making.
文摘A series of new stable (thermal and photochemical) ferrocenyl derivatives containing C=N bond and benzene ring in long conjugated chains have been synthesized and characterized by (HNMR)-H-1(400MHz), IR, and elemental analysis. Pull-push ferrocenyl complexes that we have prepared have strong NLO responses identified by electronic absorption spectrum.
基金Supported by the Natural Science Foundation of Henan Province,China(No.0611012100).
文摘Ferrocenyliminophosphine 1 and 1,1′-bisferrocenyliminophosphine 2 were easily prepared from the condensation of formylferrocene or 1,1′-diformylferrocene with 2-（diphenylphosphino） aniline. The following reduction of imine group by LiAlH4 led to the formation of the corresponding ferrocenyl amidophosphines 3 and 4. The new ligands 2- 4 were well characterized by IR, ^1H NMR, ^31p NMR spectra, elemental analysis, and ESI-MS. The catalytic activity of all the ligands with palladium compounds in the Suzuki reaction was evaluated. Ligand 1, in combination with Pd （OAc）2, was found to be the most effective for the Suzuki reaction of aryl bromides with phenylboronic acid. Typically, the use of 0. 1% （molar fraction） of Pd（OAc）2/ligand 1 in the presence of two equivalents of K2CO3 as base in toluene at 110 ℃ provided good to excellent yields of the coupled products.
文摘A new approach to fullerene ferrocenyl derivative has been made. [60]Fullerene reacts with ferrocenylmethyl azide to give N-ferrocenylmethyl imino[60]fullerene in 42% yield.
基金support by the National Natural Science Foundation of China (No.20501017)the Key Project of Chinese Ministry of Education (No.207067)the Project Sponsored by the Scientific Research Foundation for the Returned Overseas Chinese Scholars of Chinese Ministry of Education and the Student Innovation Experimental Item of Zhengzhou University.
文摘Reaction of Zn（NO3）2·6H2O with 3-（4-carboxylphenylamino）-l-ferrocenyl-2-butylen-l-one （HL） and 4,4′-bipyfidine （4,4′- bipy） in methanol solution resulted in a novel ladder-like coordination polymer {[Zn2L2（μ2-L）2（4,4′-bipy）2]·MeOH}n （1）. Its crystal structure, thermal and electrochemical properties are presented.
文摘Novel ferrocenyl derivatives of p-(10-mercaptodecyloxy) benzal 4-ferrocenylaniline have been prepared and characterized by element analysis, 1HNMR, and FAB-MS. Cyclic voltammetry has been used to characterize the self-assembled monolayers formed from the compounds on the gold electrodes.
文摘The single crystal structure of the donor-acceptor ferrocenyl derivativeC18H15ClFe (Mr = 322. 62 ) has been determined, belonging to orthorhombic crystalsystem, space group P212121 with lattice parameters a= 11. 307 (2), b= 8. 471 (2 ), c=15. 427(3) A, V= 1477. 7(9) A3, Z=4, D.= 1. 45 g. cm-3, λ(MoKα) =0. 71073A,μ= 11. 9 cm-1, F(000) = 664. The final R value for 1534 observed [I>3σ(I)] reflec-tions is 0. 060. The configuration of the C =C double bond is trans. The C5H4CH =CHC6H4Cl fragrnent is almost planar. The rings of ferrocene are almost in the eclipsedpositions with each other.
基金The financial support from the NSFC(No50873037)China Postdoctoral Science Foundation(Nos20100470908 and 201104349)the NSF of Guangdong Province(No10451064101005118)
文摘Redox-active polyelectrolyte-surfactant complexes（PSC） were prepared via the ionic self-assembly of sodium poly（styrenesulfonate） （PSS） and ferrocenyl surfactant,（11-ferrocenylundecyl）trimethylammonium bromide（FTMA） in aqueous solution. The PSS-FTMA complex exhibited an ordered interdigitated monolayer mesomorphous structure with the long period of d = 3.13 nm,and was in the ionic thermotropic liquid crystal SmA state at room temperature.Interestingly,in the solid complex, the ferrocenyl moieties formed H-aggregation showing an increase in theπ-π~＊ energy transfer of cyclopentadienes in the ferrocene moieties as known from the blue-shift in the UV spectrum.The complexes showed higher thermal stability compared with their components due to the ionic interaction.The PSS-FTMA film had a good redox reversibility,which promised to be used in electrochemical sensors.
基金Supported by the Fund for Ph.D Programme from Ministry of EducationP. R. China(980 486 2 4)
文摘Two new [60]fullerene ferrocenylmethyl derivatives have been prepared via different approaches and characterized by UV-Vis, FT-IR, NMR, FAB-MS spectra and VPO. The second approach, i.e reacting fullerene with ferrocenylmethyl azide directly, was never reported as yet.
基金supported by the National Natural Science Foundation of China(29933050)
文摘A novel chiral bis(ferrocenyl) P2N ligand 1 with C2-symmetry was synthesized through a four-step procedure from (R)-N,N-dimethyl-1-ferrocenylethylamine. In a model reaction of Pd-catalyzed allylic alkylation of 1,3-diphenylprop-2-enyl acetate 6 with dimethyl malonate, good enantioselectivity (86% e.e.) was obtained.
文摘A new type of ferrocenyl thia crown ethers used as selective ligands to some poisonous metals was synthesized, and the features of their mass spectra in electron ionization mode were summarized as: (1) the strong molecular ion peaks; (2) a characteristic homologous ion series with sequential loss of C 2H 4S or C 2H 4O from M C 5H 5; (3) a new rearrangement reaction of Fe migration; (4) the uncommon loss of alcohol or thiol from the fragments of Fe rearrangement. Some typical fragmentation patterns were discussed in detail with the aid of exact mass measurement and MS/MS technique.
文摘Much interest has been devoted to organometallic NLO materials. We have become interested in exploring the utility of ferrocenyl group as the conjugating bridge. Thus, we synthesized 1-{{[1,3-(5-methylbenzo)dithiol]-2-yli- dene}methyl}-1’-[2-(p-nitrophenyl)-(E)-ethenyl]ferrocene (1). This new ferrocenyl compound has a donor and an acceptor group in 1,1’-positions. Investigations of the solvatochromic property of the compound revealed that it has polarized structure in a polar solvent, such as DMF. SHG efficiency of the compound was estimated by an SHEW (second-harmonic generation with the evanescent wave) method.
基金supported by the National Natural Science Foundation of China (20771003)
文摘The title complex [Fc（OCH3）PS2Ir（cod）] （1, Fc = Fe（η^5-C5H4）（η^5-C5H5）, cod = 1,5-cyclooctadiene） has been prepared and characterized by X-ray diffraction analysis. It crystallizes in monoclinic, space group P21/n with a = 12.5567（5）, b = 13.5197（5）, c = 11.7833（4） A, β = 99.651（2）°, V = 1972.06（13）A^3, Z = 4, Mr = 611.52, Dc = 2.06 g/cm^3, μ（MoKα） = 7.775 mm^-, F（000） = 1184, S = 1.063, the final R = 0.0199 and wR = 0.0468 for 4063 observed reflections with I 〉 2σ（I） and 227 variables. The molecular structure of 1 shows that the central iridium atom is chelated by the [Fc（OCH3）PS2]-ligand via two sulfur atoms and coordinated by one η^4-cod molecule via four carbon atoms in a distorted octahedral coordination geometry. The average Ir-S and Ir-C bond lengths are 2.3712（8） and 2.122（3） A, respectively.
文摘The reduction reagents prepared from sodium borohydride, I-2 and a catalytic amount of chiral ferrocenyl amino alcohols 2a-e have been successfully applied to the enantioselective reduction of ketones. The optically active secondary alcohols were obtained in moderate enantiomeric excess and high chemical yield.
文摘Sodium 3-ferrocenyl-5-phenyl-pyrazoline-1-dithiocarbamate (FPPD) reacts with anhydrous rare earth chlorides in absolute ethanol to give 14 new complexes.The results of elemental analysis show that the compositions of the complexes are RE(FPPD)_3·nH_2O(RE=La,Pr～Lu and Y;n=3).The ligand and its complexes have been characterized by infrared spectroscopy,UV-visible absorption spectroscopy,~1H-NMR spectra,thermal analysis and molar conductivity measurement.
文摘The oxygen evolution reaction(OER)is a key process in water splitting for hydrogen production,yet its sluggish kinetics pose significant challenges for catalyst development.In this work,we present the first systematic study on isostructural 2D coordination polymers(CPs)based on 1,10-ferrocenediyl-bis(H-phosphinic)acid,with cobalt,manganese,and cadmium metals as electrocatalysts for OER.These polymers were synthesized via a facile solution reaction,yielding crystalline materials with excellent structural integrity.The electrocatalytic performance of CPs composites,prepared with carbon and phosphonium ionic liquid,was evaluated in 0.1 M KOH using a three-electrode system.Notably,the Co-and Cd-based CPs demonstrated exceptional OER activity,achieving an overpotential as low as 236–255 mV at 10 mA cm^(-2),surpassing those of many previously reported CP-based OER catalysts.Furthermore,these materials exhibited high stability over prolonged electrolysis,maintaining their activity without significant degradation.This work not only introduces a new class of ferrocenyl phosphinatebased CPs as highly active and durable OER catalysts but also provides valuable insights into their structureactivity relationships,paving the way for future advancements in electrocatalysis.
基金Project supported by the National Natural Science Foundation of China (No. 20172047) Henan Outstanding Youth Program 2001 and the Education Department of Henan Province.
文摘Optically active aziridino alcohols containing ferrocenyl groups were prepared from commercially available L-threonine in excellent yields and used as catalysts to promote the asymmetric addition of diethylzinc to aryalde-hydes to afford 1-arylpropanol in up to 84% enantiomeric excesses with moderate to good yields.
文摘The asymmetric reduction of prochiral ketones was catalyzed by a class of recoverable and highly stable chiral ferrocenyl amino alcohols derived from natural amino acids to yield optically active secondary alcohols in high chemical yields and moderate to good enantiomeric excesses.
