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61.
Abe F Albrow M Amidei D Anway-Wiese C Apollinari G Atac M Auchincloss P Azzi P Baden AR Bacchetta N Badgett W Bailey MW Bamberger A de Barbaro P Barbaro-Galtieri A Barnes VE Barnett BA Bauer G Baumann T Bedeschi F Behrends S Belforte S Bellettini G Bellinger J Benjamin D Benlloch J Bensinger J Beretvas A Berge JP Bertolucci S Biery K Bhadra S Binkley M Bisello D Blair R Blocker C Bodek A Bolognesi V Booth AW Boswell C Brandenburg G Brown D Buckley-Geer E Budd HS Busetto G Byon-Wagner A 《Physical review D: Particles and fields》1993,48(9):R3939-R3944
62.
Hunt G.W. Peletier M.A. Champneys A.R. Woods P.D. Ahmer Wadee M. Budd C.J. Lord G.J. 《Nonlinear dynamics》2000,21(1):3-29
A long structural system with an unstable (subcritical)post-buckling response that subsequently restabilizes typically deformsin a cellular manner, with localized buckles first forming and thenlocking up in sequence. As buckling continues over a growing number ofcells, the response can be described by a set of lengthening homoclinicconnections from the fundamental equilibrium state to itself. In thelimit, this leads to a heteroclinic connection from the fundamentalunbuckled state to a post-buckled state that is periodic. Under suchprogressive displacement the load tends to oscillate between twodistinct values.The paper is both a review and a pointer tofuture research. The response is described via a typical system, asimple but ubiquitous model of a strut on a foundation which includesinitially-destabilizing and finally-restabilizing nonlinear terms. Anumber of different structural forms, including the axially-compressedcylindrical shell, a typical sandwich structure, a model of geologicalfolding and a simple link model are shown to display such behaviour. Amathematical variational argument is outlined for determining the globalminimum postbuckling state under controlled end displacement (rigidloading). Finally, the paper stresses the practical significance of aMaxwell-load instability criterion for such systems. This criterion,defined under dead loading to be where the pre-buckled and post-buckledstate have the same energy, is shown to have significance in the presentsetting under rigid loading also. Specifically, the Maxwell load isargued to be the limit of minimum energy localized solutions asend-shortening tends to infinity. 相似文献
63.
Kadhum J. Msayib Dr. David Book Dr. Peter M. Budd Dr. Nhamo Chaukura Kenneth D. M. Harris Prof. Madeleine Helliwell Dr. Steven Tedds Allan Walton Dr. John E. Warren Dr. Mingcan Xu Dr. Neil B. McKeown Prof. 《Angewandte Chemie (International ed. in English)》2009,48(18):3273-3277
Quick on the uptake : Following its identification during a targeted search, the intriguing crystal structure of 3,3′,4,4′‐tetra(trimethylsilylethynyl)biphenyl was investigated. Simple removal of the included solvent provides an organic crystal with an open microporous structure that has a striking similarity to that of zeolite A (see picture). Reversible adsorption of nitrogen and hydrogen gases at 77 K confirms that the microporosity is permanent.
64.
Maffei AV Budd PM McKeown NB 《Langmuir : the ACS journal of surfaces and colloids》2006,22(9):4225-4229
The adsorption/desorption of N2 at 77 K and the adsorption from aqueous solution at 298 K of four organic probe molecules of different sizes (phenol, 4-nitrophenol, orange II, naphthol green B) were studied for a phthalocyanine network polymer of intrinsic microporosity (PIM) and for an activated carbon (Darco 20-40 mesh). N2 sorption analysis gave similar surface areas for the PIM and the carbon (610 and 545 m2 g(-1), respectively) but showed differences in pore size distribution, the PIM being essentially microporous (pore size < 2 nm), with a high proportion of ultramicropores (<0.7 nm), while the carbon had a broader pore size distribution, extending into the mesopore region. The carbon acted as an adsorbent for all the organic probe molecules studied, while the PIM was more selective, adsorbing the smaller molecules but rejecting the large dye naphthol green B. The PIM offers selectivity combined with a well-defined chemical structure incorporating catalytic sites. 相似文献
65.
66.
Milios CJ Manoli M Rajaraman G Mishra A Budd LE White F Parsons S Wernsdorfer W Christou G Brechin EK 《Inorganic chemistry》2006,45(17):6782-6793
The synthesis and magnetic properties of four new Mn complexes containing tripodal alcohol ligands are reported: [Mn6(OAc)6(H2tea)2(tmp)2].2MeCN (1.2MeCN), [Mn6(acac)4(OAc)2(Htmp)2(H2N-ep)2] (2), [Mn6(OAc)8(tmp)2(py)4].2py (3.2py), and [Mn6(OAc)8(thme)2(py)4].2py (4.2py) [H3tea, triethanolamine; H3tmp, 1,1,1-tris(hydroxymethyl)propane; H2N-H2ep, 2-amino-2-ethyl-1,3-propanediol; H3thme, 1,1,1-tris(hydroxymethyl)ethane]. All complexes are mixed-valent with a [Mn(III)2Mn(II)4] oxidation assignment and are constructed from four edge-sharing triangles but differ slightly in that complexes 1 and 2 display a [Mn(III)2Mn(II)4(mu2-OR)6(mu3-OR)4]4+ core, while complexes 3 and 4 feature [Mn(III)2Mn(II)4(mu2-OR)2(mu3-OR)4]8+ and [Mn(III)2Mn(II)4(mu2-OR)4(mu3-OR)4]6+ cores, respectively. dc and ac magnetic susceptibility studies in the 2-300 K range for complexes 1-4 reveal the presence of dominant antiferromagnetic exchange interactions, leading to ground states of S = 0 for 1 and 2, while complexes 3 and 4 display S = 4 ground states with D = -0.44 and -0.58 cm(-1), respectively. Single-molecule magnetism behavior was confirmed for 3 and 4 by the presence of sweep-rate and temperature-dependent hysteresis loops in single-crystal M vs H studies at temperatures down to 40 mK. Theoretical density functional calculations were used to evaluate the individual pairwise exchange interactions present, confirming the diamagnetic ground states for 1 and 2 and the S = 4 ground states for 3 and 4. 相似文献
67.
Abe F Albrow MG Amendolia SR Amidei D Antos J Anway-Wiese C Apollinari G Areti H Auchincloss P Austern M Azfar F Azzi P Bacchetta N Badgett W Bailey MW Bao J de Barbaro P Barbaro-Galtieri A Barnes VE Barnett BA Bartalini P Bauer G Baumann T Bedeschi F Behrends S Belforte S Bellettini G Bellinger J Benjamin D Benlloch J Bensinger J Benton D Beretvas A Berge JP Bertolucci S Bhatti A Biery K Binkley M Bird F Bisello D Blair RE Blocker C Bodek A Bolognesi V Bortoletto D Boswell C Boulos T 《Physical review D: Particles and fields》1994,50(5):2966-3026
68.
Abe F Albrow M Amidei D Anway-Wiese C Apollinari G Atac M Auchincloss P Azzi P Bacchetta N Baden AR Badgett W Bailey MW Bamberger A de Barbaro P Barbaro-Galtieri A Barnes VE Barnett BA Bauer G Baumann T Bedeschi F Behrends S Belforte S Bellettini G Bellinger J Benjamin D Benlloch J Bensinger J Beretvas A Berge JP Bertolucci S Biery K Bhadra S Binkley M Bisello D Blair R Blocker C Bodek A Bolognesi V Booth AW Boswell C Brandenburg G Brown D Buckley-Geer E Budd HS Busetto G Byon-Wagner A 《Physical review D: Particles and fields》1994,50(9):5518-5534
69.
Abe F Albrow M Amidei D Anway-Wiese C Apollinari G Atac M Auchincloss P Azzi P Bacchetta N Baden AR Badgett W Bailey MW Bamberger A de Barbaro P Barbaro-Galtieri A Barnes VE Barnett BA Bauer G Baumann T Bedeschi F Behrends S Belforte S Bellettini G Bellinger J Benjamin D Benlloch J Bensinger J Beretvas A Berge JP Bertolucci S Biery K Bhadra S Binkley M Bisello D Blair R Blocker C Bloom K Bodek A Bolognesi V Booth AW Boswell C Brandenburg G Brown D Buckley-Geer E Budd HS Busetto G Byon-Wagner A 《Physical review D: Particles and fields》1994,49(1):R1-R6
70.
Abe F Albrow M Amidei D Anway-Wiese C Apollinari G Areti H Auchincloss P Azfar F Azzi P Bacchetta N Badgett W Bailey MW Bao J de Barbaro P Barbaro-Galtieri A Barnes VE Barnett BA Bartalini P Bauer G Baumann T Bedeschi F Behrends S Belforte S Bellettini G Bellinger J Benjamin D Benlloch J Benton D Beretvas A Berge JP Bertolucci S Bhatti A Biery K Binkley M Bird F Bisello D Blair RE Blocker C Bodek A Bolognesi V Bortoletto D Boswell C Boulos T Brandenburg G Buckley-Geer E Budd HS Burkett K 《Physical review letters》1994,72(22):3456-3460