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1.
Copper(II)‐Mediated Self‐Assembly of Hairpin Peptides and Templated Synthesis of CuS Nanowires
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Chengdong Wang Dr. Yawei Sun Dr. Jiqian Wang Prof. Hai Xu Prof. Jian R. Lu 《化学:亚洲杂志》2015,10(9):1953-1958
The self‐assembly of peptides and proteins under well‐controlled conditions underlies important nanostructuring processes that could be harnessed in practical applications. Herein, the synthesis of a new hairpin peptide containing four histidine residues is reported and the self‐assembly process mediated by metal ions is explored. The work involves the combined use of circular dichroism, NMR spectroscopy, UV/Vis spectroscopy, AFM, and TEM to follow the structural and morphological details of the metal‐coordination‐mediated folding and self‐assembly of the peptide. The results indicate that by forming a tetragonal coordination geometry with four histidine residues, copper(II) ions selectively trigger the peptide to fold and then self‐assemble into nanofibrils. Furthermore, the copper(II)‐bound nanofibrils template the synthesis of CuS nanowires, which display a near‐infrared laser‐induced thermal effect. 相似文献
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Ferroelectric Coordination Polymers Self‐Assembled from Mesogenic Zinc(II) Porphyrin and Dipolar Bridging Ligands
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Dr. Joseph K.‐H. Hui Hiroyuki Kishida Keita Ishiba Kenta Takemasu Dr. Masa‐aki Morikawa Prof. Dr. Nobuo Kimizuka 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(40):14213-14218
A new class of ferroelectric coordination‐based polymers has been developed by the self‐assembly of lipophilic zinc porphyrin ( ZnP ) and ditopic bridging ligands. The ligands contain dipolar benzothiadiazole or fluorobenzene units, which are axially coordinated to ZnP with the dipole moments oriented perpendicular to the coordination axes. The coordination‐based polymers show ferroelectric characteristics in the liquid crystalline state, as revealed by distinctive hysteresis in the polarization–electric field (P–E) loops and inversion current peaks in current–voltage (I–V) loops. The observed ferroelectric properties are explainable by flip–flop rotation of the dipolar axle ligands induced by the applied electric field, as demonstrated by the positive‐up–negative‐down (PUND) measurements. The present system provides a new operating principle in supramolecular ferroelectrics. 相似文献
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Yiming Wang Zhi Xu Matija Lovrak Vincent A. A. le Sage Kai Zhang Xuhong Guo Rienk Eelkema Eduardo Mendes Jan H. van Esch 《Angewandte Chemie (International ed. in English)》2020,59(12):4830-4834
Supramolecular structures with strain‐stiffening properties are ubiquitous in nature but remain rare in the lab. Herein, we report on strain‐stiffening supramolecular hydrogels that are entirely produced through the self‐assembly of synthetic molecular gelators. The involved gelators self‐assemble into semi‐flexible fibers, which thereby crosslink into hydrogels. Interestingly, these hydrogels are capable of stiffening in response to applied stress, resembling biological intermediate filaments system. Furthermore, strain‐stiffening hydrogel networks embedded with liposomes are constructed through orthogonal self‐assembly of gelators and phospholipids, mimicking biological tissues in both architecture and mechanical properties. This work furthers the development of biomimetic soft materials with mechanical responsiveness and presents potentially enticing applications in diverse fields, such as tissue engineering, artificial life, and strain sensors. 相似文献
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Xiangyuan Ouyang Meifang Wang Linjie Guo Chengjun Cui Ting Liu Yongan Ren Yan Zhao Zhilei Ge Xiniu Guo Gang Xie Jiang Li Chunhai Fan Lihua Wang 《Angewandte Chemie (International ed. in English)》2020,59(29):11836-11844
Fluorescent copper nanoclusters (CuNCs) have been widely used in chemical sensors, biological imaging, and light‐emitting devices. However, individual fluorescent CuNCs have limitations in their capabilities arising from poor photostability and weak emission intensities. As one kind of aggregation‐induced emission luminogen (AIEgen), the formation of aggregates with high compactness and good order can efficiently improve the emission intensity, stability, and tunability of CuNCs. Here, DNA nanoribbons, containing multiple specific binding sites, serve as a template for in situ synthesis and assembly of ultrasmall CuNCs (0.6 nm). These CuNC self‐assemblies exhibit enhanced luminescence and excellent fluorescence stability because of tight and ordered arrangement through DNA nanoribbons templating. Furthermore, the stable and bright CuNC assemblies are demonstrated in the high‐sensitivity detection and intracellular fluorescence imaging of biothiols. 相似文献
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Inspired by nacre that is mechanically strong and versatile in light manipulation, large‐scale black films with a nacre‐like microstructure and carbon nanotube inclusion were prepared using a facile self‐assembly technique. A layered structure promoting blackness and toughness simultaneously was realized, affording robust films with a solar–absorptivity as high as 96.9%. Our design strategy and fabrication process will be beneficial for the facile access to various advanced blackbody coatings. 相似文献
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Ftima Aparicio Paula B. Chamorro Raquel Chamorro Santiago Casado David Gonzlez‐Rodríguez 《Angewandte Chemie (International ed. in English)》2020,59(39):17091-17096
Despite the central importance of aqueous amphiphile assemblies in science and industry, the size and shape of these nano‐objects is often difficult to control with accuracy owing to the non‐directional nature of the hydrophobic interactions that sustain them. Here, using a bioinspired strategy that consists of programming an amphiphile with shielded directional Watson–Crick hydrogen‐bonding functions, its self‐assembly in water was guided toward a novel family of chiral micelle nanotubes with partially filled lipophilic pores of about 2 nm in diameter. Moreover, these tailored nanotubes are successfully demonstrated to extract and host molecules that are complementary in size and chemical affinity. 相似文献
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《化学:亚洲杂志》2017,12(2):224-232
Poly(γ‐benzyl‐l ‐glutamate)‐block‐poly(ethylene glycol) (PBLG‐b ‐PEG) rod–coil block copolymers and poly(γ‐benzyl‐l ‐glutamate) (PBLG) homopolymers can cooperatively self‐assemble into superhelical structures in aqueous solution. Herein, we discovered that the helices can have multiple strands with tunable characteristics. The strand number was dependent on the initial polymer concentration of the self‐assembly, the self‐assembly temperature, and the weight fraction of the block copolymers in the mixture. Higher initial polymer concentrations or lower weight fractions of the block copolymers induced the formation of helices with larger diameters and higher strand numbers, and helices prepared at higher temperatures had higher strand numbers. Based on an analysis of the correlation between the geometric parameters of the helices and the strand number, a possible mechanism for the formation of multistranded superhelices is suggested. 相似文献
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Rindia M. Putri Prof. Jeroen J. L. M. Cornelissen Dr. Melissa S. T. Koay 《Chemphyschem》2015,16(5):911-918
Proteins and protein‐based assemblies represent the most structurally and functionally diverse molecules found in nature. Protein cages, viruses and bacterial microcompartments are highly organized structures that are composed primarily of protein building blocks and play important roles in molecular ion storage, nucleic acid packaging and catalysis. The outer and inner surface of protein cages can be modified, either chemically or genetically, and the internal cavity can be used to template, store and arrange molecular cargo within a defined space. Owing to their structural, morphological, chemical and thermal diversity, protein cages have been investigated extensively for applications in nanotechnology, nanomedicine and materials science. Here we provide a concise overview of the most common icosahedral viral and nonviral assemblies, their role in nature, and why they are highly attractive scaffolds for the encapsulation of functional materials. 相似文献
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A novel 1D copper(II) helical chain is constructed through the connection of tetranuclear copper(II) units [Cu4(L)(Py)4] (H8L=N,N′‐(BINOL‐3,3′‐dicarboxyl)‐disalicylhydrazide, where BINOL is 1,1′‐binaphthalenyl‐2,2′‐diol, py=pyridine) by weak coordination‐driven self‐assembly, and characterized by IR, single crystal X‐ray diffraction, thermogravimetric analysis, and X‐ray power diffraction analysis. Interestingly, the helical chains are packed in an alternating left‐(M) and right‐handed (P) chirality, the orientation of the helices was determined by the axial chirality of the ligand. The complex shows antiferromagnetic interactions between the copper centers. 相似文献
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Direct Synthesis of a Covalently Self‐Assembled Peptide Nanogel from a Tyrosine‐Rich Peptide Monomer and Its Biomineralized Hybrids
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Dr. Kyoung‐Ik Min Dong‐Hwi Kim Hyune‐Jea Lee Prof. Dr. Liwei Lin Prof. Dr. Dong‐Pyo Kim 《Angewandte Chemie (International ed. in English)》2018,57(20):5630-5634
There has been significant progress in the self‐assembly of biological materials, but the one‐step covalent peptide self‐assembly for well‐defined nanostructures is still in its infancy. Inspired by the biological functions of tyrosine, a covalently assembled fluorescent peptide nanogel is developed by a ruthenium‐mediated, one‐step photo‐crosslinking of tyrosine‐rich short peptides under the visible light within 6 minutes. The covalently assembled peptide nanogel is stable in various organic solvents and different pH levels, unlike those made from vulnerable non‐covalent assemblies. The semipermeable peptide nanogel with a high density of redox‐active tyrosine acts as a novel nano‐bioreactor, allowing the formation of uniform metal–peptide hybrids by selective biomineralization under UV irradiation. As such, this peptide nanogel could be useful in the design of novel nanohybrids and peptidosomes possessing functional nanomaterials. 相似文献
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Antara Reja Syed Pavel Afrose Dibyendu Das 《Angewandte Chemie (International ed. in English)》2020,59(11):4329-4334
Early evolution benefited from a complex network of reactions involving multiple C?C bond forming and breaking events that were critical for primitive metabolism. Nature gradually chose highly evolved and complex enzymes such as lyases to efficiently facilitate C?C bond formation and cleavage with remarkable substrate selectivity. Reported here is a lipidated short peptide which accesses a homogenous nanotubular morphology to efficiently catalyze C?C bond cleavage and formation. This system shows morphology‐dependent catalytic rates, suggesting the formation of a binding pocket and registered enhancements in the presence of the hydrogen‐bond donor tyrosine, which is exploited by extant aldolases. These assemblies showed excellent substrate selectivity and templated the formation of a specific adduct from a pool of possible adducts. The ability to catalyze metabolically relevant cascade transformations suggests the importance of such systems in early evolution. 相似文献
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Dr. Olga V. Makhlynets Pallavi M. Gosavi Prof. Dr. Ivan V. Korendovych 《Angewandte Chemie (International ed. in English)》2016,55(31):9017-9020
We have shown that de novo designed peptides self‐assemble in the presence of copper to create supramolecular assemblies capable of carrying out the oxidation of dimethoxyphenol in the presence of dioxygen. Formation of the supramolecular assembly, which is akin to a protein fold, is critical for productive catalysis since peptides possessing the same functional groups but lacking the ability to self‐assemble do not catalyze substrate oxidation. The ease with which we have discovered robust and productive oxygen activation catalysts suggests that these prion‐like assemblies might have served as intermediates in the evolution of enzymatic function and opens the path for the development of new catalyst nanomaterials. 相似文献
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Two novel supramolecular complexes [Cu(bpapa)(dhbd)]·CHaOH (1) and [Cu(bpapa)(ma)]·ma (2) (bpapa= bis[6-(2-pyridylamino)pyrid-2-yl]amine, dhbd=2,3-dihydroxybutanedioate dianion, ma=a-methacrylate) were rationally designed, synthesized and characterized by single crystal X-ray diffraction, IR, electronic spectroscopy and thermogravimetric analyses. Complex 1 was the first oligo-a-pyfidylamino complex based on hydroxypolycarboxylate and self-assembled into a 3D honeycomb configuration network with open channels and tubes containing 1D ladder-shaped double chains formed by hydrogen bonds and aromatic π-π stacking interactions. Complex 2 constructed a 2D supramolecular network extended by 1D chains from dimeric supramolecular synthon through noncovalent supramolecular interactions. In the two complexes, the chelating monohelical ligand adopted all-anti configuration. Density functional theory calculations were applied to 1 and 2. 相似文献
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Supramolecular Polymers Self‐Assembled from trans‐Bis(pyridine) Dichloropalladium(II) and Platinum(II) Complexes
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Mingming Chen Chengsha Wei Jiaojiao Tao Xibo Wu Dr. Ningdong Huang Prof. Dr. Guobin Zhang Prof. Dr. Liangbin Li 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(10):2812-2818
Two structurally similar trans‐bis(pyridine) dichloropalladium(II)‐ and platinum(II)‐type complexes were synthesized and characterized. They both self‐assemble in n‐hexane to form viscous fluids at lower concentrations, but form metallogels at sufficient concentrations. The viscous solutions were studied by capillary viscosity measurements and UV/Vis absorption spectra monitored during the disassembly process indicated that a metallophilic interaction was involved in the supramolecular polymerization process. For the two supramolecular assemblies, uncommon continuous porous networks were observed by using SEM and TEM revealed that they were built from nanofibers that fused and crosslinked with the increase of concentration. The xerogels of the palladium and platinum complexes were carefully studied by using synchrotron radiation WAXD and EXAFS. The WAXD data show close stacking distances driven by π–π and metal–metal interactions and an evident dimer structure for the platinum complex was found. The coordination bond lengths were extracted from fitting of the EXAFS data. Moreover, close PtII–PtII (PdII–PdII) and Pt?Cl (Pd?Cl) interactions proposed from DFT calculations in the reported oligo(phenylene ethynylene) (OPE)‐based palladium(II) pyridyl supramolecular polymers were also confirmed by using EXAFS. The PtII–PtII interaction is more feasible for supramolecular interaction than the PdII–PdII interaction in our simple case. 相似文献
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Programmable Self‐Assembly of Heterometallic Palladium(II)–Copper(II) 1D Grid‐Chain using Dinuclear Palladium(II) Corners with Pyrazole–Carboxylic Acid Ligands
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Wen‐Qing Sun Dr. Jin Tong Hong‐Lin Lu Ting‐Ting Ma Dr. Hong‐Wei Ma Prof. Dr. Shu‐Yan Yu 《化学:亚洲杂志》2018,13(9):1108-1113
A novel heterometallic diPdII–diCuII grid‐chain, {[(bpy)4Pd4Cu2L4](NO3)4}n ( 2 ; bpy=2,2′‐bipyridine), was synthesized through a programmable self‐assembly approach from the molecular corners [(bpy)2Pd2(HL)(L)](NO3) ( 1 ) as linkers with CuII nitrate by using the bifunctional H2L ligand featuring primary (pyrazole) and secondary (benzoic acid) groups. Structural analysis revealed that 1D structure 2 consists of one [Cu2(O2CPh)4]n unit as a bridge and two [(bpy)2Pd2L2]n corners. Additionally, the catalytic effect of the heterometallic synergy on the Suzuki coupling reaction by using 2 was further explored. 相似文献
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Qing Bian Wenshuo Wang Guoxiang Han Yupeng Chen Prof. Dr. Shutao Wang Prof. Dr. Guojie Wang 《Chemphyschem》2016,17(16):2503-2508
Stimuli‐responsive surfaces that can regulate and control cell adhesion have attracted much attention for their great potential in diverse biomedical applications. Unlike for pH‐ and temperature‐responsive surfaces, the process of photoswitching requires no additional input of chemicals or thermal energy. In this work, two different photoresponsive azobenzene films are synthesized by chemisorption and electrostatic layer‐by‐layer (LbL) assembly techniques. The LbL film exhibits a relatively loose packing of azobenzene chromophores compared with the chemisorbed film. The changes in trans/cis isomer ratio of the azobenzene moiety and the corresponding wettability of the LbL films are larger than those of the chemisorbed films under UV light irradiation. The tendency for cell adhesion on the LbL films decreases markedly after UV light irradiation, whereas adhesion on the chemisorbed films decreases only slightly, because the azobenzene chromophores stay densely packed. Interestingly, the tendency for cell adhesion can be considerably increased on rough substrates, the roughness being introduced by use of photolithography and inductively coupled plasma deep etching techniques. For the chemisorbed films on rough substrates, the amount of cells that adhere also changes slightly after UV light irradiation, whereas, the amount of cells that adhere to LbL films on rough substrates decreases significantly. 相似文献