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91.
In the current contribution, we present a multi-scale constitutive model capturing macroscopic inelastic effects (like stress softening and permanent set) in soft tissues under cyclic loading. Soft biological tissues can be described as a biological composite material. The extracellular matrix is hereby reinforced by collagen fibers which themself are an assembly of collagen fibrils embedded in a proteoglycan (PG) rich matrix. Micro-damage induced by cyclic loading is treated by an interaction scenario between the fibrils and the PGs. At the low strain regime PGs promote sliding between fibrils [1] which leads to the yielding of statistical distributed overlapping segments. The breakage of the PG-bridges is defined by a decreasing PG-density. Due to the accumulated damage of the PG connections at high tissue strains, the strains at the fibril level increases. This finally drives the over-stretching of the fibrils, which is associated with a permanent rupture of the hydrogen bonds inside of the tropocollagen molecules [2]. The so obtained model is in line with recent experimental findings [1, 2] and was additionally validated against experimental data available in literature. (© 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)  相似文献   
92.
The first total synthesis of resveratrone and iso-resveratrone based on an epoxide olefination approach is described. The pivotal reaction proceeds by insertion of the lithiated epoxide into a boronic ester and subsequent syn-elimination. Resveratrone has been described to have remarkable photophysical properties, including two-photon absorption. Therefore, an azide derivative has been prepared to allow for use as a biological label.  相似文献   
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Anew initiative to facilitate interdisciplinary research on advanced materials, biomaterials, and nanotechnology has begun operation in Europe. CERIC, the Central European Research Infrastructure Consortium, is a partnership between two synchrotrons and seven other advanced, user-based research centers, each in a different country participating in the consortium (see Figure 1).  相似文献   
95.
Several new benzoate ester derivatives of ethyl α-hydroxymethylacrylate were synthesized using phase transfer catalysis and found to display unexpectedly rapid photopolymerization; i.e., from 2 to 8 times faster than MMA. New derivatives described here include the 4-fluoro-, 4-trifluoromethyl-, 4-methyl-, 2-hydroxy-, 4-nitro-, 4-methoxy-, 4-cyano-, and 3,4,5-trimethoxybenzoate esters along with the parent benzoate ester. Relative reactivities of these monomers in photopolymerizations were compared with those of the nonaromatic formate, acetate, hexanoate, and stearate derivatives. Reactivities of the nonaromatic ester derivatives increased with the length of the side chain while for the more reactive aromatic esters, rates increased in the order 4-methyl-, 4-fluoro- and benzoate < 4-trifluoromethyl- and 2-hydroxy- < 4-cyano- < 4-methoxy- < 3,4,5-trimethoxybenzoate. Tgs of the benzoate polymers ranged from 125°C for the 4-fluoro to 163°C for the 4-cyanobenzoate while those of the alkyl ester derivatives ranged from 15 to 78°C. Number average molecular weights of photoinitiated polymers (ca 10,000–20,000) were lower than those found for bulk and solution polymers (20,000—708,000) consistent with higher radical concentrations from photoinitiation. These materials greatly expand the number of candidates available for rapid photocure in thin film and coating applications, especially because their physical properties are those of linear rather than highly crosslinked structures formed from multifunctional systems. © 1996 John Wiley & Sons, Inc.  相似文献   
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Here we present a combined experimental and theoretical study on the secondary structure of isolated proteins as a function of charge state. In infrared spectra of the proteins ubiquitin and cytochrome c, amide I (C=O stretch) and amide II (N–H bend) bands can be found at positions that are typical for condensed‐phase proteins. For high charge states a new band appears, substantially red‐shifted from the amide II band observed at lower charge states. The observations are interpreted in terms of Coulomb‐driven transitions in secondary structures from mostly helical to extended C5‐type hydrogen‐bonded structures. Support for this interpretation comes from simple energy considerations as well as from quantum chemical calculations on model peptides. This transition in secondary structure is most likely universal for isolated proteins that occur in mass spectrometric experiments.  相似文献   
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99.
We present experimental evidence for the spontaneous formation of a macroscopic spin polarization in overlapping regions of two independent Bose-Einstein condensates produced in different hyperfine states of 87Rb. The condensates are independent in the sense that we do not explicitly introduce a relative phase between them. A single "spin-tip" pulse maps the transverse spin polarization into longitudinal spin polarization, and the atomic density distributions are measured with a Stern-Gerlach imaging method. The resulting matter-wave interference patterns are anticorrelated.  相似文献   
100.
We report a resonantly fiber-laser-pumped Er:YAG laser operating at the eye-safe wavelength of 1645 nm, exhibiting 43% optical efficiency and 54% incident slope efficiency and emitting 7-W average power when repetitively Q switched at 10 kHz. To our knowledge, this is the best performance (conversion efficiency and average power) obtained from a bulk solid-state Q-switched erbium laser. At a 1.1-kHz pulse repetition frequency the laser produces 3.4-mJ pulses with a corresponding peak power of 162 kW. Frequency doubling to produce 822.5-nm, 4.7-kW pulses at 10 kHz was performed to demonstrate the laser's utility.  相似文献   
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