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1 (i.e. helical, tetrahedral, cubic and other polyhedra).
2 fullerene-topology cage built from 28 uranyl polyhedra.
3 orated into the self-assembled symmetric DNA polyhedra.
4 ations of that involve two different regular polyhedra.
5 s formed from linked M(O,F)(n) and P(O,F)(n) polyhedra.
6 truncated octahedron, one of the Archimedean polyhedra.
7 ut also for determining the alignment of the polyhedra.
8 or Ca/Au/Bi mixtures to give 16-atom Friauf polyhedra.
9 of bridging ligands in soluble metal-organic polyhedra.
10 octahedra are completely surrounded by IO(3) polyhedra.
11 nd other topologies containing as many as 60 polyhedra.
12 ahedra, each of which is bonded to six IO(3) polyhedra.
13 iO(6) octahedron that is linked to six IO(3) polyhedra.
14 use any net change in the metal coordination polyhedra.
15 dral symmetry only in half of the individual polyhedra.
16 dues based on calculations with Voronoi-like polyhedra.
17 red static arrays of tiles, linked rings and polyhedra.
18 nt diol dehydratase is associated with these polyhedra.
19 lin inclusions but many fewer than wild-type polyhedra.
20 ching rules for the assembly of Frank-Kasper polyhedra.
21 (12-) , featuring three carbonate-ligated Nb-polyhedra.
22 ionality analysis method by means of Voronoi polyhedra.
23 network of 4-, 5-, and 6-coordinated AlO(x) polyhedra.
24 rranged in overlayed Archimedean or Platonic polyhedra.
25 can be cured and purified to yield colloidal polyhedra.
26 ional structure of corner-shared Al(BO3 )3 O polyhedra.
27 we construct a reference library of regular polyhedra.
28 nation common to smaller and higher-symmetry polyhedra.
29 he discs occupying the faces in the caveolar polyhedra.
30 shared atoms between two linked coordination polyhedra.
31 sional structure of corner-shared Mg(CO3)2F2 polyhedra.
32 sting of corner- and edge-shared UF9 and MF6 polyhedra.
33 produced diverse synthetic three-dimensional polyhedra.
34 engths was used for hierarchical assembly of polyhedra.
35 polyhedra and the relative lack of irregular polyhedra.
36 shell cluster consisting of 68 uranyl peroxo polyhedra, 16 nitrate groups, and ~44 K(+) and Na(+) cat
37 e II porous liquids (PLs) from metal-organic polyhedra, a kind of excellent porous molecular sources,
38 nd orientation, we explore how five distinct polyhedra-a tetrahedron, an octahedron, a cube, a cuboct
40 y corner-sharing capped trigonal planar AgO4 polyhedra, AgO6 capped square pyramids, and AgO6 octahed
43 suited to the functional requirements of the polyhedra and has been either preserved or re-selected d
44 agonal assembly of 25 Zr-oxy/peroxo/hydroxyl polyhedra and is the largest Zr/Hf cluster topology iden
45 he basic structures for linking squares into polyhedra and networks (reticulation) are enumerated, an
46 (2+) ions preferably occupy RbO(6) and YO(6) polyhedra and show the characteristic red emission band
48 gher ratio of corner-sharing to edge-sharing polyhedra and that exhibit highly localized electronic b
49 particular the abundance of regular Voronoi polyhedra and the relative lack of irregular polyhedra.
50 cavities in these double-shell metal-organic polyhedra and their inner/outer binding sites provide pe
54 synthesis of colloidal SnS cubes, spherical polyhedra, and sheets and demonstrate their activity for
55 ple for maximizing the yield of self-folding polyhedra; and (ii) shortest paths from 2D nets to 3D po
56 individually within cubic inclusion bodies (polyhedra, approximately 100 nm across), although two to
57 iency (AQE) of 6.1 % for OER compared to the polyhedra (AQE: 1.6 %) and SrTaO2 N polycrystals (AQE: 0
60 ayer of TiO(2) stoichiometry in which TiO(5) polyhedra are arranged into edge-shared structures, in c
62 hombic polyhedra, the 6gon faces in Goldberg polyhedra are equilateral and planar but not equiangular
63 also the fact that the 9-coordinated CeO(9) polyhedra are expected to be geometrically more complian
65 ous responses of single atoms and also major polyhedra are found to change greatly with increasing ex
66 cturally related to corundum, but the AlO(6) polyhedra are highly distorted, with the interatomic bon
72 ted GaO(4), four-connected GaO(4) and GaO(6) polyhedra are probed for the parent La(3)Ga(5)GeO(14) st
73 4, where topological low coordination number polyhedra are still observed around the critical cavity.
75 protein crystals, termed occlusion bodies or polyhedra, are dense protein assemblies that form a crys
76 dra, including some Archimedean and Platonic polyhedra, arise spontaneously in elastic shells formed
78 e group Cmcm) features the same coordination polyhedra around tin and lithium as previously predicted
80 ormulate the generation of dense packings of polyhedra as an optimization problem, using an adaptive
83 single-crystalline nanoboxes of gold: hollow polyhedra bounded by six [100] and eight [111] facets.
84 arge-transfer excitation distorts the TiO(6) polyhedra by altering the local charge density occupancy
85 hows that monodisperse, atomically smooth Ag polyhedra can self-assemble into uniform interparticle g
86 ties from those of the initial metal-organic polyhedra can thus lead to new metal-organic polyhedra w
89 The structure consists of REO6 and REO2F4 polyhedra connected by Si4O10 sheets with a previously u
90 s a mixture of distorted Ti-O(5) and Ti-O(6) polyhedra connected via 71% corner-sharing and 23% edge-
93 tachment of cucurbit[n]uril to metal organic polyhedra constitutes a promising vehicle for the develo
94 method of positioning the dividing plane in polyhedra construction, and (iv) the set of structures u
95 led edges characteristic of wild-type AcMNPV polyhedra, contained fractures, and occluded few virions
96 tructure can be viewed as nested, concentric polyhedra, containing a total of five forms of Archimede
97 such as porous organic cages, metal-organic polyhedra, covalent organic frameworks and zeotype mater
98 on and structure determination of nano-sized polyhedra crystal (PhC) at a high resolution of 1.80 ang
100 th Bergman clusters emerging as Ca-Cd Friauf polyhedra (derived from the MgZn2-type CaCd2 phase) enca
101 assembly of size-controlled triply periodic polyhedra, discrete variants of the Primitive, Diamond,
103 nstructed from totally face-enclosed organic polyhedra displaying a precise uniform micropore size of
105 es in these systems have a signature Voronoi polyhedra distribution that is defined by lognormal curv
106 ar proteins by approximating them to various polyhedra (dodecahedron, truncated octahedron, icosahedr
107 al embeddings of the edge-graphs of Platonic polyhedra, {f, z}, where f, z denote the number of edges
108 -prepared Sr2 Ta2 O7 nanoplates and SrTaO2 N polyhedra form by flux-assisted nitridation of the nanop
109 olds of Wigner-Seitz cells with many-faceted polyhedra, forming an important bridge between the simpl
110 The analysis extends to the "theta(z) " polyhedra, [Formula: see text] The vertices of these sym
111 d to study the chemical bonding in the boron polyhedra found in other structures including neutral bi
112 these PF mutants exhibited the traits of few polyhedra (FP) mutants; however, no large DNA insertions
116 metallosupramolecular cages known as M12L24 polyhedra have been adapted to serve as nanometer-scale
117 sses comprising continuously linked [AlO(x)] polyhedra have been prepared in only a few systems under
119 tubifying the edges of conventional Platonic polyhedra, have (chiral) symmetries 2fz (I, O, and T), w
120 king Platonic, Archimedean and even Goldberg polyhedra, however, nesting multiple polyhedra in one cl
121 polyhedra overlap with those of the Platonic polyhedra; however, their helicity requires curvilinear
124 of manipulating the chemistry of homoleptic polyhedra in heteroanionic compounds for electronic stru
125 by kinetic pathways comprising distorted Li polyhedra in metastable intermediates along two-phase bo
127 oldberg polyhedra, however, nesting multiple polyhedra in one cluster is challenging, not only for sy
129 c interference zones are limited to isolated polyhedra in the 1, 2 and 4 positions and the alpha face
131 ; and (ii) shortest paths from 2D nets to 3D polyhedra in the configuration space are important for r
134 features edge-sharing between the Ti and Bi polyhedra, in contrast to the dominant corner-linking of
136 tion metal compounds composed of homoanionic polyhedra, including nitrides, oxides, and fluorides.
137 We show here that irregular and regular polyhedra, including some Archimedean and Platonic polyh
138 the 5 Platonic polyhedra, the 13 Archimedean polyhedra--including the truncated icosahedron or soccer
139 ves rise to new sulfur-centered coordination polyhedra, increases structural inhomogeneity, changes e
141 cture adopted by the SnS cubes and spherical polyhedra is expanded along the a and b axes and contrac
143 on, the rearrangement of the Fe coordination polyhedra is unique such that all available FeOn units (
145 comprises bicapped trigonal prismatic PuS(8) polyhedra linked in chains through edge-sharing interact
147 or channels lined with fluoride ions, metal polyhedra, M(O,F)(n), linked through vertex, edge, or fa
149 lf-assembled Pd(12)L(24) metal-organic cages/polyhedra (MOCs): simple mixing of a catalyst-ligand of
150 rst superassembly of nanosized metal-organic polyhedra (MOP) and their biomimetic coatings of lipid b
151 (isophthalic acid)(24) Cu(24) metal-organic polyhedra (MOP) as a core protected by 24 polymer chains
153 polar n-dodecyl-functionalized metal-organic polyhedra (MOP-18) in polar liquid pillar[5]arene (P5-L)
155 he synthesis of this series of metal-organic polyhedra (MOPs) employs sulfate-capped oxygen-centered
159 -linking DNA with Rh(II)-based metal-organic polyhedra (MOPs), which entails coordination of DNA to t
163 'glue' to link organic ligands together into polyhedra.Most of the architectures employed thus far ha
164 space-filling arrangements of most discrete polyhedra nanostructures of the same shape is not possib
165 oublets, triangles, and tetrahedra to exotic polyhedra not found in infinite lattice packings, molecu
166 shape measures analysis of the coordination polyhedra of a host of transition metal complexes with b
167 enyl) links to yield five highly crystalline polyhedra of general formula [NH2(CH3)2]8[Fe12O4(-)(SO4)
168 erein the reconfiguration of the system into polyhedra of increasing volume asymmetry delays the onse
169 that will enforce the formation of specific polyhedra of metals within the core of the structure.
172 le, we entropically reshape the coordination polyhedra of the particles in the system, a change that
174 loying pre-selected 0-periodic metal-organic polyhedra or 2-periodic metal-organic layers, SBBs or SB
176 unique relationship between edge-transitive polyhedra or layers and minimal edge-transitive 3-period
177 n into more elaborate building units (namely polyhedra or layers) to (i) elucidate the unique relatio
178 ext] The vertices of these symmetric tangled polyhedra overlap with those of the Platonic polyhedra;
180 ed RE clusters are replaced by metal-organic polyhedra, peripherally functionalized so as to have the
181 ded virions (odv-e25, odv-e66, odv-e18), and polyhedra (polyhedrin/granulin, p10, pp34, and fp25k).
182 erefore, remarkable that both AcMNPV and CPV polyhedra possess identical crystal lattices and crystal
183 n be viewed as a combination of coordination polyhedra present in the nearest binary phases in the Ca
185 eometries, those containing 24 and 28 uranyl polyhedra, respectively, show that the capsules-like clu
187 system is littered, however, with distorted polyhedra-shards of rock and ice produced by ubiquitous
188 ected at distances suggesting that Am and Fe polyhedra share corners in geometries ranging from bent
190 f this structure to baculovirus or cypovirus polyhedra shows a distinct protein structure, crystal sp
194 ells with two elastic components buckle into polyhedra such as dodecahedra, octahedra, tetrahedra, an
195 and empty (no RNA) capsids were found inside polyhedra, suggesting a spontaneous RNA encapsidating pr
196 ree-dimensional arrangement of Ca(-COO, -OH) polyhedra supporting one-dimensional pores with aperture
197 ed by the disruption of connectivity between polyhedra (TaO6 octahedra or TaO7 bipyramids) at the par
198 he structure into 'natural tiles' or Voronoi polyhedra that are metastable and, consequently, tempora
199 for one-step self-assembly of wireframe DNA polyhedra that are more massive than most previous struc
201 ality of the number of discrete coordination polyhedra that constitute the structural building units
202 eferred structures for four families of hard polyhedra that match, in every instance, previous simula
203 ined in terms of the "cross-bracing" between polyhedra that occurs as a result of the phase transitio
204 f Tl tetrahedra along c are constructed from polyhedra that share opposed like edges, and these are i
206 dic anion-vacancy order to generate multiple polyhedra that together with cation order produce a pola
207 ahedral, and icosahedral--are the 5 Platonic polyhedra, the 13 Archimedean polyhedra--including the t
209 n number architectures starting from regular polyhedra through pseudosymmetrization of trimeric build
210 tegy based on space-filling tessellations of polyhedra to create three-dimensional reconfigurable mat
212 metalates, polyoxocations, and metal-organic polyhedra), to the mesoscale (supramolecular assembly pr
213 The starting material, crystalline PtNi3 polyhedra, transforms in solution by interior erosion in
214 the connection of isolated LnO(6)(H(2)O)(3) polyhedra (tricapped trigonal prism) through the mellita
215 the capsid changes from spherical to faceted polyhedra, two modes are necessary to accomplish the con
216 roup, and unit cell dimensions, however, all polyhedra utilise common principles of occlusion body as
217 gands and building blocks of condensed metal polyhedra, we recently reported a one-dimensional nickel
218 bound together: self-assembled symmetric DNA polyhedra were used to organize proteins in 3D space.
219 triperoxide or uranyl dihydroxidediperoxide polyhedra, were only realized within the last decade.
221 ructure of corner-shared MgO4, PO4, and TeO6 polyhedra, which form a [TeMg3P2O14]infinity framework.
222 ar capsids than wild type and more irregular polyhedra, which tend to be larger than in the wild type
226 us, truncated tetrahedral and heterocuboidal polyhedra, whose pore size and functionality can be syst
227 l graphs are those of the classical Platonic polyhedra, whose symmetries are *2fz, according to Conwa
229 rising corner-sharing PbCl(4)(eta(2)-COO)(2) polyhedra with bridging equatorial chlorides and termina
230 l assemblies of molecules are packed to form polyhedra with coordination numbers 12, 14, 15 or 16.
231 polyhedra can thus lead to new metal-organic polyhedra with distinct properties (including size and s
232 ent here suggests that we can design faceted polyhedra with diverse symmetries by coassembling opposi
234 wever, stereospecific assembly of artificial polyhedra with mechanical properties and guest-binding a
236 ereby extending the ability to functionalize polyhedra with nanobodies in a desired stoichiometry.
238 Selective occupation of Eu(2+) in inorganic polyhedra with small coordination numbers results in bro
240 es, including irregular, asymmetric DX-based polyhedra with variable edge lengths and vertices demons
243 nt network of As(V)/P coordinated to Fe(III) polyhedra, with varying amounts of Ca bound directly and
244 the smallest cytoplasmic polyhedrosis virus polyhedra yet characterized, which we failed to solve at