Current research progress of photopolymerized hydrogels in tissue engineering

Owing to the special fo rmation of photopolymerized hydrogels,they can effectively control the formation of hydrogels in space and time.Moreover,the photopolymerized hydrogels have mild formation conditions and biocompatibility;therefore,they can be widely used in tissue engineering.With the development and application of manufacturing technology,photopolymerized hydrogels can be widely used in cell encapsulation,scaffold materials,and other tissue engineering fields through more elaborate manufacturing methods.This review covers the types of photoinitiators,manu facturing technologies for photopolymerized hydrogels as well as the materials used,and a summary of the applications of photopolymerized hydrogels in tissue engineering.     

Bio-inspired and Eco-friendly Synthesis of 3D Spongy Meso-Microporous Carbons from CO2 for Supercapacitors

Inspired by the spongy bone structures, three-dimensional (3D) sponge-like carbons with meso-microporous structures are synthesized through one-step electro-reduction of CO₂ in molten carbonate Li₂CO₃−Na₂CO₃−K₂CO₃ at 580 °C. SPC4-0.5 (spongy porous carbon obtained by electrolysis of CO₂ at 4 A for 0.5 h) is synthesized with the current efficiency of 96.9 %. SPC4-0.5 possesses large electrolyte ion accessible surface area, excellent wettability and electronical conductivity, ensuring the fast and effective mass and charge transfer, which make it an advcanced supercapacitor electrode material. SPC4-0.5 exhibits a specific capacitance as high as 373.7 F g⁻¹ at 0.5 A g⁻¹, excellent cycling stability (retaining 95.9 % of the initial capacitance after 10000 cycles at 10 A g⁻¹), as well as high energy density. The applications of SPC4-0.5 in quasi-solid-state symmetric supercapacitor and all-solid-state flexible devices for energy storage and wearable piezoelectric sensor are investigated. Both devices show considerable capacitive performances. This work not only presents a controllable and facile synthetic route for the porous carbons but also provides a promising way for effective carbon reduction and green energy production.     

High‐Nuclear Organometallic Copper(I)–Alkynide Clusters: Thermochromic Near‐Infrared Luminescence and Solution Stability

Cu(CF₃COO)₂ reacts with tert‐butylacetylene (tBuC≡CH) in methanol in the presence of metallic copper powder to give two air‐stable clusters, [Cu^I₁₅(tBuC≡C)₁₀(CF₃COO)₅]?tBuC≡CH ( 1 ) and [Cu^I₁₆(tBuC≡C)₁₂(CF₃COO)₄(CH₃OH)₂] ( 2 ). The assembly process involves in situ comproportionation reaction between Cu²⁺ and Cu⁰ and the formation of two different clusters is controlled by reactants concentration. The clusters consist of Cu₁₅ and Cu₁₆ cores co‐stabilized by strong by σ‐ and π‐bonded tert‐butylethynide and CF₃COO^? (together with methanol molecule in 2 ). Their stabilities in solution were confirmed using electrospray ionization mass spectrometry in which the cluster core remains intact for 1 in chloroform and acetone, and for 2 in acetonitrile. Strong thermochromic luminescence in the near infrared (NIR) region was observed in the solid‐state. Of particular interest, the emission maximum of 1 is red‐shifted from 710 nm at 298 K to 793 nm at 93 K, along with a 17‐fold fluorescence enhancement. In contrast, 2 exhibits red shift from 298 to 123 K followed by blue shift from 123 to 93 K. The emission wavelength was correlated with the structural parameters using variable‐temperature X‐ray single‐crystal analyses. The rich cuprophilic interaction plays a significant role in the formation of ³LMCT (tBuC≡C→Cu_x) excited state mixed with cluster‐centered (³CC) characters, which can be considerably influenced by temperature, leading to thermochromic luminescence. The present work provides 1) a new synthetic protocol for the high‐nuclear Cu^I–alkynyl clusters; 2) a comprehensive insight into the mechanism of thermochromic luminescence; 3) unusual emissive materials with the characters of NIR and thermochromic luminescence simultaneously.     

强磁场条件下Mn-Sb梯度复合材料的制备

研究了Mn-898wt%Sb合金在无磁场以及磁场为B=88 T、不同强度的磁场梯度作用下的凝固组织变化，并分析了上述不同强磁场条件对合金凝固组织影响的作用机理.研究表明，在较大梯度磁场作用时，试样中出现了初生MnSb相与Sb相以及共晶组织共存的现象，而且初生MnSb相与Sb相产生了明显的分层现象.此外，磁场梯度作用下初生MnSb相和Sb相的含量随着磁场梯度的增大而增加.论文对初生MnSb相和Sb相的分离机理进行了探讨，发现在梯度磁场作用下，熔融金属中不同磁化率的合金组元团簇受力不同，造成     

Operatorenkalkül über freien Monoiden III: Lagrangeinversion und Sheffersysteme

In this part the relations between the theory of binomial systems for noncommuting variables (of part II) and the results ofRota, Cigler et al. for the commutative case are studied in some detail. Afterwards for binomial systems of diagonal type there are given generalizations of the Rodrigues formula and the theorem ofLagrange-Good. A short development of Sheffer sequences follows. Finally the results are extended to binomial systems the structure of which is determined by any partial order of linear type.     

Synthesis of aminothiazole derived morphinans

Two aminothiazole derived morphinans 9 and 11 were prepared for our ongoing opioid ligands study. The synthesis was initiated from levorphanol 1, which was first triflated, and then subjected to Pd-catalyzed reduction followed by nitration. The resulting two nitrated isomers were characterized by analogy to known compounds. The formation of the aminothiazole ring occurred highly selectively to yield only one product from each of the anilines 6 and 7.     

衬底对Cu(In,Ga)Se2薄膜织构的影响

分别在苏打石灰玻璃、Mo箔、无择优取向的Mo薄膜以及(110)择优取向的Mo薄膜四种不同衬底上，采用共蒸发工艺沉积约2 μm厚的Cu(In,Ga)Se₂薄膜，用X射线衍射仪测量薄膜的织构，研究衬底对Cu(In,Ga)Se₂薄膜织构的影响.在以上四种衬底上沉积的Cu(In,Ga)Se₂薄膜的(112)衍射峰强度依次逐渐减弱，(220/204)衍射峰从无到有且强度逐渐增强.在苏打石灰玻璃和Mo箔衬底上的Cu(In,Ga)Se_{2关键词： 择优取向 Cu(In 2}薄膜')" href="#">Ga)Se₂薄膜 太阳电池     

Nd-Fe-B/FeCo多层纳米复合膜的结构和磁性

制备了Nd₂₈Fe₆₆B₆/Fe₅₀Co₅₀多层纳米复合磁性薄膜，对溅射态和650℃退火处理15 min试样的相成分分析和微结构的观察显示，溅射态薄膜呈非晶态，经650℃退火处理15 min后，薄膜主要相成分为硬磁性Nd₂Fe₁₄B相和软磁性相FeCo(110)相.Nd₂Fe₁₄B相呈柱状，其易磁化c轴垂直于膜面，尺寸约10 nm.在硬磁性相和软磁性相之间存在少量富Nd相和非晶态，富Nd相大小约7 nm.磁性测量和分析表明，1)该系列薄膜退火态具有垂直于膜面的磁晶各向异性.2)对于固定厚度(10 nm)层Nd-Fe-B和不同厚度(t_FeCo=1—100 nm)层FeCo多层纳米复合膜,剩磁随软磁相FeCo 厚度的增加快速增加，而矫顽力则减小.当t_FeCo=5 nm时，最大磁能积达到200 kJ/m³. 3)硬磁相Nd-Fe-B层和软磁相FeCo层之间交换耦合导致剩磁和磁能积增强. 关键词： Nd-Fe-B/FeCo多层纳米复合膜 交换耦合 磁各向异性