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1.
Hexa‐peri‐hexabenzocoronene (HBC) is a discotic‐shaped conjugated molecule with strong π–π stacking property, high intrinsic charge mobility, and good self‐assembly properties. For a long time, however, organic photovoltaic (OPV) solar cells based on HBC demonstrated low power conversion efficiencies (PCEs). In this study, two conjugated terpolymers, poly[N‐9′‐heptadecanyl‐2,7‐carbazole‐alt‐5,5′‐(4′,7′‐di‐2‐thienyl‐2′,1′,3′‐benzothiadiazole)] (PCDTBT)‐ 5 HBC and PCDTBT‐ 10 HBC, were synthesized by incorporating different amounts of HBC as the third component into poly[N‐9′‐heptadecanyl‐2,7‐carbazole‐alt‐5,5′‐(4′,7′‐di‐2‐thienyl‐2′,1′,3′‐benzothiadiazole)] (PCDTBT) through Suzuki coupling polymerization. For comparison, the donor–acceptor (D –A) conjugated dipolymer PCDTBT was also synthesized to investigate the effect of HBC units on conjugated polymers. The HBC‐containing polymers exhibited higher thermal stabilities, broader absorption spectra, and lower highest‐occupied molecular orbital (HOMO) energy levels. In particular, the field‐effect mobilities were enhanced by more than one order of magnitude after the incorporation of HBC into the conjugated polymer backbone on account of increased interchain π–π stacking interactions. The bulk heterojunction (BHJ) polymer solar cells (PSCs) fabricated with the polymers as donor and PC71BM as acceptor demonstrated gradual improvement of open‐circuit voltage (VOC) and short‐circuit current (JSC) with the increase in HBC content. As a result, the PCEs were improved from 3.21 % for PCDTBT to 3.78 % for PCDTBT‐ 5 HBC and then to 4.20 % for PCDTBT‐ 10 HBC.  相似文献   

2.
A water‐soluble surfactant consisting of hexa‐peri‐hexabenzocoronene (HBC) as hydrophobic aromatic core and hydrophilic carboxy substituents was synthesized. It exhibited a self‐assembled nanofiber structure in the solid state. Profiting from the π interactions between the large aromatic core of HBC and graphene, the surfactant mediated the exfoliation of graphite into graphene in polar solvents, which was further stabilized by the bulky hydrophilic carboxylic groups. A graphene dispersion with a concentration as high as 1.1 mg L?1 containing 2–6 multilayer nanosheets was obtained. The lateral size of the graphene sheets was in the range of 100–500 nm based on atomic force microscope (AFM) and transmission electron microscope (TEM) measurements.  相似文献   

3.
Herein we report the synthesis and photophysical and supramolecular properties of a novel three‐dimensional capsule‐like hexa‐peri‐hexabenzocoronene (HBC)‐containing carbon nanocage, tripodal‐[2]HBC, which is the first synthetic model of capped zigzag [12,0] carbon nanotubes (CNTs). Tripodal‐[2]HBC was synthesized by the palladium‐catalyzed coupling of triboryl hexabenzocoronene and L‐shaped cyclohexane units, followed by nickel‐mediated C−Br/C−Br coupling and subsequent aromatization of the cyclohexane moieties. The physical properties of tripodal‐[2]HBC and its supramolecular host–guest interaction with C70 were further studied by UV/Vis and fluorescence spectroscopy. Theoretical calculations revealed that the strain energy of tripodal‐[2]HBC was as high as 55.2 kcal mol−1.  相似文献   

4.
Herein we report the synthesis and photophysical and supramolecular properties of a novel three‐dimensional capsule‐like hexa‐peri‐hexabenzocoronene (HBC)‐containing carbon nanocage, tripodal‐[2]HBC, which is the first synthetic model of capped zigzag [12,0] carbon nanotubes (CNTs). Tripodal‐[2]HBC was synthesized by the palladium‐catalyzed coupling of triboryl hexabenzocoronene and L‐shaped cyclohexane units, followed by nickel‐mediated C?Br/C?Br coupling and subsequent aromatization of the cyclohexane moieties. The physical properties of tripodal‐[2]HBC and its supramolecular host–guest interaction with C70 were further studied by UV/Vis and fluorescence spectroscopy. Theoretical calculations revealed that the strain energy of tripodal‐[2]HBC was as high as 55.2 kcal mol?1.  相似文献   

5.
Novel hexa‐peri‐hexabenzocoronene (HBC) derivatives, FHBC and FHBC*, which carry perfluoroalkyl segments on one side of the HBC core and long alkyl tails on the other, were synthesized. Their perfluoroalkyl segments are highly solvated in C6F6 (solvophilic effect) and do not assemble, whereas in CH2Cl2, they are excluded (solvophobic effect) and assemble together consequently. For example, the use of C6F6 and CH2Cl2 as assembling media for FHBC leads to the selective formation of single‐ and multi‐walled nanotubes, respectively. When a higher monomer concentration is applied in CH2Cl2, multi‐walled nanotubes with a larger number of walls result. FHBC in CH2Cl2 self‐assembles rather slowly, thereby allowing for the observation of coil‐on‐tube structures, which are possible intermediates for the stepwise radial growth of the nanotubular wall. Casting of the multi‐walled nanotubes onto a quartz plate yields a superhydrophobic thin film with a water contact angle of 161±2°.  相似文献   

6.
Two types of three‐arm and four‐arm, star‐shaped poly(D,L ‐lactic acid‐alt‐glycolic acid)‐b‐poly(L ‐lactic acid) (D,L ‐PLGA50‐b‐PLLA) were successfully synthesized via the sequential ring‐opening polymerization of D,L ‐3‐methylglycolide (MG) and L ‐lactide (L ‐LA) with a multifunctional initiator, such as trimethylolpropane and pentaerythritol, and stannous octoate (SnOct2) as a catalyst. Star‐shaped, hydroxy‐terminated poly(D,L ‐lactic acid‐alt‐glycolic acid) (D,L ‐PLGA50) obtained from the polymerization of MG was used as a macroinitiator to initiate the block polymerization of L ‐LA with the SnOct2 catalyst in bulk at 130 °C. For the polymerization of L ‐LA with the three‐arm, star‐shaped D,L ‐PLGA50 macroinitiator (number‐average molecular weight = 6800) and the SnOct2 catalyst, the molecular weight of the resulting D,L ‐PLGA50‐b‐PLLA polymer linearly increased from 12,600 to 27,400 with the increasing molar ratio (1:1 to 3:1) of L ‐LA to MG, and the molecular weight distribution was rather narrow (weight‐average molecular weight/number‐average molecular weight = 1.09–1.15). The 1H NMR spectrum of the D,L ‐PLGA50‐b‐PLLA block copolymer showed that the molecular weight and unit composition of the block copolymer were controlled by the molar ratio of L ‐LA to the macroinitiator. The 13C NMR spectrum of the block copolymer clearly showed its diblock structures, that is, D,L ‐PLGA50 as the first block and poly(L ‐lactic acid) as the second block. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 40: 409–415, 2002  相似文献   

7.
Materials based upon hexa‐peri‐hexabenzocoronenes (HBCs) show significant promise in a variety of photovoltaic applications. There remains the need, however, for a soluble, versatile, HBC‐based platform, which can be tailored by incorporation of electroactive groups or groups that can prompt self‐assembly. The synthesis of a HBC–fluorene hybrid is presented that contains an expanded graphitic core that is highly soluble, resists aggregation, and can be readily functionalized at its vertices. This new HBC platform can be tailored to incorporate six electroactive groups at its vertices, as exemplified by a facile synthesis of a representative hexaaryl derivative of FHBC. Synthesis of new FHBC derivatives, containing electroactive functional groups that can allow controlled self‐assembly, may serve as potential long‐range charge‐transfer materials for photovoltaic applications.  相似文献   

8.
Materials based upon hexa‐peri‐hexabenzocoronenes (HBCs) show significant promise in a variety of photovoltaic applications. There remains the need, however, for a soluble, versatile, HBC‐based platform, which can be tailored by incorporation of electroactive groups or groups that can prompt self‐assembly. The synthesis of a HBC–fluorene hybrid is presented that contains an expanded graphitic core that is highly soluble, resists aggregation, and can be readily functionalized at its vertices. This new HBC platform can be tailored to incorporate six electroactive groups at its vertices, as exemplified by a facile synthesis of a representative hexaaryl derivative of FHBC. Synthesis of new FHBC derivatives, containing electroactive functional groups that can allow controlled self‐assembly, may serve as potential long‐range charge‐transfer materials for photovoltaic applications.  相似文献   

9.
Two complexes based on the ligand 1,4‐dihydro‐2,3‐quinoxalinedione, namely [Mn(H2L)2(H2O)2]n ( 1 ) and {[Zn2(H2L)2(tz)2] · 5H2O}n ( 2 ) (H3L = 2,3‐dioxo‐1,2,3,4‐tetrahydroquinoxaline‐6‐carboxylic acid, Htz = 1,2,4‐triazole) were hydrothermally synthesized and characterized by elemental analyses, IR spectroscopy, as well as single‐crystal and powder X‐ray diffraction. Complex 1 exhibited a 1D comb‐like chain formed by H2L anions linking MnII ions, whereas complex 2 was a 2D layer‐like structure with square‐shaped windows and outstretched arms built by combination of H2L and tz ligands with ZnII ions. The adjacent chains or layers connected with each other by intermolecular hydrogen bonding and π–π stacking to further extend to a 3D supermolecular framework. In addition, the thermal stabilities, luminescence properties, and optical energy gap of 1 and 2 were investigated in detail.  相似文献   

10.
The known glucaro‐1,5‐lactam 8 , its diastereoisomers 9 – 11 , and the tetrahydrotetrazolopyridine‐5‐carboxylates 12 – 14 were synthesised as potential inhibitors of β‐D ‐glucuronidases and α‐L ‐iduronidases. The known 2,3‐di‐O‐benzyl‐4,6‐O‐benzylidene‐D ‐galactose ( 16 ) was transformed into the D ‐galactaro‐ and L ‐altraro‐1,5‐lactams 9 and 11 via the galactono‐1,5‐lactam 21 in twelve steps and in an overall yield of 13 and 2%, respectively. A divergent strategy, starting from the known tartaric anhydride 41 , led to the D ‐glucaro‐1,5‐lactam 8 , D ‐galactaro‐1,5‐lactam 9 , L ‐idaro‐1,5‐lactam 10 , and L ‐altraro‐1,5‐lactam 11 in ten steps and in an overall yield of 4–20%. The anhydride 41 was transformed into the L ‐threuronate 46 . Olefination of 46 to the (E)‐ or (Z)‐alkene 47 or 48 followed by reagent‐ or substrate‐controlled dihydroxylation, lactonisation, azidation, reduction, and deprotection led to the lactams 8 – 11 . The tetrazoles 12 – 14 were prepared in an overall yield of 61–81% from the lactams 54, 28 , and 67 , respectively, by treatment with Tf2O and NaN3, followed by saponification, esterification, and hydrogenolysis. The lactams 8 – 11 and 40 and the tetrazoles 12 – 14 are medium‐to‐strong inhibitors of β‐D ‐glucuronidase from bovine liver. Only the L ‐ido‐configured lactam 10 (Ki = 94 μM ) and the tetrazole 14 (Ki = 1.3 mM ) inhibit human α‐L ‐iduronidase.  相似文献   

11.
A cyclophane is reported incorporating two units of a heptagon‐containing extended polycyclic aromatic hydrocarbon (PAH) analogue of the hexa‐peri‐hexabenzocoronene (HBC) moiety (hept‐HBC). This cyclophane represents a new class of macrocyclic structures that incorporate for the first time seven‐membered rings within extended PAH frameworks. The saddle curvature of the hept‐HBC macrocycle units induced by the presence of the nonhexagonal ring along with the flexible alkyl linkers generate a cavity with shape complementarity and appropriate size to enable π interactions with fullerenes. Therefore, the cyclophane forms host–guest complexes with C60 and C70 with estimated binding constants of Ka=420±2 m ?1 and Ka=(6.49±0.23)×103 m ?1, respectively. As a result, the macrocycle can selectively bind C70 in the presence of an excess of a mixture of C60 and C70.  相似文献   

12.
Herein we report the organoplatinum‐mediated bottom‐up synthesis, characterization, and properties of a novel large π‐extended carbon nanoring based on a nanographene hexa‐peri ‐hexabenzocoronene (HBC) building unit. This tubular structure can be considered as an example of the longitudinal extension of the cycloparaphenylene scaffold to form a large π‐extended carbon nanotube (CNT) segment. The cyclic tetramer of a tetramesityl HBC ([4]CHBC) was synthesized by the reaction of a 2,11‐diborylated hexa‐peri ‐hexabenzocoronene with a platinum complex, followed by reductive elimination. The structure of this tubular molecule was further confirmed by physical characterization. Theoretical calculations indicate that the strain energy of this nanoring is as high as 49.18 kcal mol−1. The selective supramolecular host–guest interaction between [4]CHBC and C70 was also investigated.  相似文献   

13.
Herein we report the organoplatinum‐mediated bottom‐up synthesis, characterization, and properties of a novel large π‐extended carbon nanoring based on a nanographene hexa‐peri ‐hexabenzocoronene (HBC) building unit. This tubular structure can be considered as an example of the longitudinal extension of the cycloparaphenylene scaffold to form a large π‐extended carbon nanotube (CNT) segment. The cyclic tetramer of a tetramesityl HBC ([4]CHBC) was synthesized by the reaction of a 2,11‐diborylated hexa‐peri ‐hexabenzocoronene with a platinum complex, followed by reductive elimination. The structure of this tubular molecule was further confirmed by physical characterization. Theoretical calculations indicate that the strain energy of this nanoring is as high as 49.18 kcal mol−1. The selective supramolecular host–guest interaction between [4]CHBC and C70 was also investigated.  相似文献   

14.
Abstract. Two bis‐triazole‐bis‐amide‐based copper(II) pyridine‐2,3‐dicarboxylate coordination polymers (CPs), [Cu(2,3‐pydc)(dtb)0.5(DMF)] · 2H2O ( 1 ) and [Cu(2,3‐pydc)(dth)0.5(DMF)] · 2H2O ( 2 ) (2,3‐H2pydc = pyridine‐2,3‐dicarboxylic acid, dtb = N,N′‐bis(4H‐1,2,4‐triazole)butanamide, and dth = N,N′‐bis(4H‐1,2,4‐triazole)hexanamide), were synthesized under solvothermal conditions. CPs 1 and 2 show similar two‐dimensional (2D) structures. In 1 , the 2,3‐pydc anions bridge the CuII ions into a one‐dimensional (1D) chain. Such 1D chains are linked by the dtb ligands to form a 2D layer. The adjacent 2D layers are extended into a three‐dimensional (3D) supramolecular architecture by hydrogen‐bonding interactions. The electrochemical properties of 1 and 2 were investigated.  相似文献   

15.
The synthesis of a hexa‐peri‐hexabenzocoronene (HBC) with a central borazine core is described. The solid‐state structure of this BN‐doped HBC (BN‐HBC) is isotypic with that of the parent HBC. Scanning tunneling microscopy shows that BN‐HBC lies flat on Au(111) in a two‐dimensional pattern.  相似文献   

16.
Two 5‐methyl‐tetrazolate (mtz)‐based paramagnetic metal coordination polymers, {[Cu2(H2O)2(mtz)(μ3‐OH)(nip)] · H2O}n ( 1 ) and [Cu(H2O)(mtz)2]n ( 2 ), were obtained in the presence and absence of aromatic 5‐nitroisophathalate (nip2–) coligand by varying the preparation methods. Structural determinations reveal that 1 is a three‐dimensional (3D) framework with corner‐sharing triangular ribbons infinitely extended by ditopic nip2– connectors. In contrast, 2 is a coplanar (4,4) layer constructed from square‐pyramidal CuII ions and μ‐N1,N4‐mtz linkers, which is further assembled into a 3D supramolecular network by interlayer hydrogen‐bonding interactions. Magnetically, spin‐frustrated antiferromagnetic ordering is observed in the 3D framework of 1 and canted antiferromagnetic behavior with a slight spin‐flop transition is presented in 2 , which are structurally resulting from the locally Δ‐ribbon in 1 and asymmetric magnetic superexchange mediated by the μ‐N1,N4‐mtz bridge of 2 .  相似文献   

17.
D ,L ‐3‐Methylglycolide (MG) was synthesized via two step reactions with a good yield (42%). It was successfully polymerized in bulk with stannous octoate as a catalyst at 110 °C. The effects of the polymerization time and catalyst concentration on the molecular weight and monomer conversion were studied. Poly(D ,L ‐lactic acid‐co‐glycolic acid) (D ,L ‐PLGA50; 50/50 mol/mol) copolymers were successfully synthesized from the homopolymerization of MG with high polymerization rates and high monomer conversions under moderate polymerization conditions. 1H NMR spectroscopy indicated that the bulk ring‐opening polymerization of MG conformed to the coordination–insertion mechanism. 13C NMR spectra of D ,L ‐PLGA50 copolymers obtained under different experimental conditions revealed that the copolymers had alternating structures of lactyl and glycolyl. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 4179–4184, 2000  相似文献   

18.
An efficient and facile synthesis of phytosphingosine and dihydrosphingosine derivatives is described with less steps and in improved overall yield (66–72%) starting from commercially available tri‐O‐benzyl‐D ‐galactal. The key steps include Wittig reaction, Mitsunobu transformation, reduction, and deprotection.  相似文献   

19.
Living ω‐aluminum alkoxide poly‐ϵ‐caprolactone and poly‐D,L ‐lactide chains were synthesized by the ring‐opening polymerization of ϵ‐caprolactone (ϵ‐CL) and D,L ‐lactide (D,L ‐LA), respectively, and were used as macroinitiators for glycolide (GA) polymerization in tetrahydrofuran at 40 °C. The P(CL‐b‐GA) and P(LA‐b‐GA) diblock copolymers that formed were fractionated by the use of a selective solvent for each block and were characterized by 1H NMR spectroscopy and differential scanning calorimetry analysis. The livingness of the operative coordination–insertion mechanism is responsible for the control of the copolyester composition, the length of the blocks, and, ultimately, the thermal behavior. Because of the inherent insolubility of the polyglycolide blocks, microphase separation occurs during the course of the sequential polymerization, resulting in a stable, colloidal, nonaqueous copolymer dispersion, as confirmed by photon correlation spectroscopy. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 39: 294–306, 2001  相似文献   

20.
Four metal‐organic coordination polymers [Cd(4‐bpcb)1.5Cl2(H2O)] ( 1 ), [Cd(4‐bpcb)0.5(mip)(H2O)2] · 3H2O ( 2 ), [Co(4‐bpcb)(oba)(H2O)2] ( 3 ), and [Ni(4‐bpcb)(oba)(H2O)2] ( 4 ) [4‐bpcb = N,N′‐bis(4‐pyridinecarboxamide)‐1, 4‐benzene, H2mip = 5‐methylisophthalic acid, and H2oba = 4, 4′‐oxybis(benzoic acid)] were synthesized under hydrothermal conditions and characterized by single‐crystal X‐ray diffraction, elemental analyses, IR spectroscopy, powder X‐ray diffraction, and TG analysis. In complex 1 , two Cl anions serve as bridges to connect two Cd‐(μ1‐4‐bpcb) subunits forming a dinuclear unit, which are further linked by μ2‐bridging 4‐bpcb to generate 1D zigzag chain. Complex 2 shows a 2D 63 network constructed by [Cd‐mip]n zigzag chains and μ2‐bridging 4‐bpcb ligands. Complexes 3 and 4 are isostructural 2D (4, 4) grid networks derived from [M‐oba]n (M = Co, Ni) zigzag chains and [M‐(4‐bpcb)]n linear chains. The 1D chains for 1 and the 2D networks for 2 – 4 are finally extended into 3D supramolecular architectures by hydrogen bonding interactions. The roles of dicarboxylates and central metal ions on the assembly and structures of the target compounds were discussed. Moreover, the thermal stabilities, photoluminescent properties, and photocatalytic activities of complexes 1 – 4 and the electrochemical properties of complexes 3 and 4 were investigated.  相似文献   

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