hush

WordNet

wash by removing particles; "Wash ores"
(poetic) tranquil silence; "the still of the night" (同)stillness, still
cause to be quiet or not talk; "Please silence the children in the church!" (同)quieten, silence, still, shut up, hush up
become quiet or still; fall silent; "hush my baby!"
run water over the ground to erode (soil), revealing the underlying strata and valuable minerals
silence (someone) by uttering `shush!
a bribe paid to someone to insure that something is kept secret
deep-fried cornbread ball (southern) (同)hushpuppy
in a softened tone; "hushed voices"; "muted trumpets"; "a subdued whisper"; "a quiet reprimand" (同)muted, subdued, quiet

PrepTutorEJDIC

(特に騒ぎ・騒音のあとの)『静けさ』 / …‘を'『静かにさせる』,黙らせて(…)させる《+『名』+『to』+『名』》 / 静かにする,黙る / シーッ,静かに,黙れ
(沈黙を命じて)シッ(hush)・…‘に'シッと言って黙らせる
フライケーキ(米南部でとうもろこしの粉で作り油で軒げた菓子)
(計画などが)極秘の,内密の

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/12/09 15:32:20」(JST)

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English Journal

Neonatal immunity: Hush-a by baby.

Bordon Y.
Nature reviews. Immunology.Nat Rev Immunol.2014 Jan;14(1):4-5. doi: 10.1038/nri3584. Epub 2013 Dec 6.
PMID 24310086

Electronic Communication in Linear Oligo(azobenzene) Radical Anions.

Moneo A, Justino GC, Carvalho MF, Oliveira MC, Antunes AM, Bléger D, Hecht S, Telo JP.Author information Centro de Química Estrutural, Instituto Superior Técnico, Universidade de Lisboa , Av. Rovisco Pais, 1049-001 Lisboa, Portugal.AbstractThe radical anions of five bis(azobenzene) and one tris(azobenzene) compounds were studied by optical and electron paramagnetic resonance (EPR) spectroscopies in polar aprotic solvents. The radicals with planar or almost-planar bridges are charge-delocalized mixed-valence species. Localization of charge occurs only on radicals with highly twisted biphenyl bridges. The electronic coupling between the azobenzene charge-bearing units, calculated as half the energy of the intervalence band for the charge-delocalized and by the Hush equation for the charge-localized radicals, decreases with the distance and torsion angle between azobenzene units. These radicals have smaller electronic couplings between charge-bearing units than other mixed-valence organic radicals with similar bridges. However, the application of a three-stage model to the tris(azobenzene) radical anion intervalence band yields an electronic coupling between consecutive azobenzenes that is higher than in any of the bis(azobenzene) radicals studied.
The journal of physical chemistry. A.J Phys Chem A.2013 Dec 27;117(51):14056-64. doi: 10.1021/jp407099c. Epub 2013 Dec 5.
The radical anions of five bis(azobenzene) and one tris(azobenzene) compounds were studied by optical and electron paramagnetic resonance (EPR) spectroscopies in polar aprotic solvents. The radicals with planar or almost-planar bridges are charge-delocalized mixed-valence species. Localization of ch
PMID 24308386

A multiscale simulation technique for molecular electronics: design of a directed self-assembled molecular n-bit shift register memory device.

Lambropoulos NA, Reimers JR, Crossley MJ, Hush NS, Silverbrook K.Author information CSIRO Energy Technology, Life Sciences Centre, 11 Julius Avenue, North Ryde, NSW, 2113, Australia. School of Chemistry, The University of Sydney, Sydney, NSW, 2006, Australia.AbstractA general method useful in molecular electronics design is developed that integrates modelling on the nano-scale (using quantum-chemical software) and on the micro-scale (using finite-element methods). It is applied to the design of an n-bit shift register memory that could conceivably be built using accessible technologies. To achieve this, the entire complex structure of the device would be built to atomic precision using feedback-controlled lithography to provide atomic-level control of silicon devices, controlled wet-chemical synthesis of molecular insulating pillars above the silicon, and controlled wet-chemical self-assembly of modular molecular devices to these pillars that connect to external metal electrodes (leads). The shift register consists of n connected cells that read data from an input electrode, pass it sequentially between the cells under the control of two external clock electrodes, and deliver it finally to an output device. The proposed cells are trimeric oligoporphyrin units whose internal states are manipulated to provide functionality, covalently connected to other cells via dipeptide linkages. Signals from the clock electrodes are conveyed by oligoporphyrin molecular wires, and μ-oxo porphyrin insulating columns are used as the supporting pillars. The developed multiscale modelling technique is applied to determine the characteristics of this molecular device, with in particular utilization of the inverted region for molecular electron-transfer processes shown to facilitate latching and control using exceptionally low energy costs per logic operation compared to standard CMOS shift register technology.
Nanotechnology.Nanotechnology.2013 Dec 20;24(50):505202. doi: 10.1088/0957-4484/24/50/505202. Epub 2013 Nov 22.
A general method useful in molecular electronics design is developed that integrates modelling on the nano-scale (using quantum-chemical software) and on the micro-scale (using finite-element methods). It is applied to the design of an n-bit shift register memory that could conceivably be built usin
PMID 24270608

Efficient Electronic Communication of Two Ruthenium Centers through a Rigid Ditopic N-Heterocyclic Carbene Linker.

Nussbaum M, Schuster O, Albrecht M.Author information Department of Chemistry, University of Fribourg, Chemin du Musée 9, 1700 Fribourg (Switzerland).AbstractA ditopic benzobis(carbene) ligand precursor was prepared that contained a chelating pyridyl moiety to ensure co-planarity of the carbene ligand and the coordination plane of a bound octahedral metal center. Bimetallic ruthenium complexes comprising this ditopic ligand [L4 Ru-C,N-bbi-C,N-RuL4 ] were obtained by a transmetalation methodology (C,N-bbi-C,N=benzobis(N-pyridyl-N'-methyl-imidazolylidene). The two metal centers are electronically decoupled when the ruthenium is in a pseudotetrahedral geometry imparted by a cymene spectator ligand (L4 =[(cym)Cl]). Ligand exchange of the Cl(-) /cymene ligands for two bipyridine or four MeCN ligands induced a change of the coordination geometry to octahedral. As a consequence, the ruthenium centers, separated through space by more than 10 Å, become electronically coupled, which is evidenced by two distinctly different metal-centered oxidation processes that are separated by 134 mV (L4 =[(bpy)2 ]; bpy=2,2'-bipyridine) and 244 mV (L4 =[(MeCN)4 ]), respectively. Hush analysis of the intervalence charge-transfer bands in the mixed-valent species indicates substantial valence delocalization in both complexes (delocalization parameter Γ=0.41 and 0.37 in the bpy and MeCN complexes, respectively). Spectroelectrochemical measurements further indicated that the mixed-valent Ru(II) /Ru(III) species and the fully oxidized Ru(III) /Ru(III) complexes gradually decompose when bound to MeCN ligands, whereas the bpy spectators significantly enhance the stability. These results demonstrate the efficiency of carbenes and, in particular, of the bbi ligand scaffold for mediating electron transfer and for the fabrication of molecular redox switches. Moreover, the relevance of spectator ligands is emphasized for tailoring the degree of electronic communication through the benzobis(carbene) linker.
Chemistry (Weinheim an der Bergstrasse, Germany).Chemistry.2013 Dec 16;19(51):17517-27. doi: 10.1002/chem.201302688. Epub 2013 Nov 11.
A ditopic benzobis(carbene) ligand precursor was prepared that contained a chelating pyridyl moiety to ensure co-planarity of the carbene ligand and the coordination plane of a bound octahedral metal center. Bimetallic ruthenium complexes comprising this ditopic ligand [L4 Ru-C,N-bbi-C,N-RuL4 ] were
PMID 24218243

Japanese Journal

Hush...Hush, Sweet Charlotte

阿部和重
早稲田文学. [第10次] (8), 289-299, 2014
NAID 40020166649

『鏡の国のアリス』の3つの眠りと2つの夢 : "Hush-a-by lady, in Alice's lap!" の子守歌から始めて

夏目康子
清泉女子大学人文科学研究所紀要 (34), 205-219, 2013
NAID 40019719286

A Key Factor for Ultrafast Rates of Photoinduced Electron Transfer among Five Flavin Mononucleotide Binding Proteins: Effect of Negative, Positive, and Neutral Charges at Residue 13 on the Rate

Taniguchi Seiji,Chosrowjan Haik,Tanaka Fumio,Nakanishi Takeshi,Sato Shuta,Haruyama Yoshihiro,Kitamura Masaya
Bulletin of the Chemical Society of Japan 86(3), 339-350, 2013
… The observed lifetimes of the five FMN-bp isoforms were simultaneously analyzed with both Marcus and Hush, and Kakitani and Mataga ET theories, in order to characterize the ET mechanisms. …
NAID 130004059063

効率的なURLフィルタリング方式に関する一検討(データ転送方式)

河野伸也,今野雅之,森岡千晴 [他],山本太三
電子情報通信学会技術研究報告. NS, ネットワークシステム 111(468), 415-420, 2012-03-01
近年、社会的な要請により、不適切サイトの閲覧規制が通信事業者に求められてきている。また、未成年者に対して有害サイトの閲覧を規制するペアレンタルコントロールサービスがインターネットサービスプロバイダにより提供されることが一般的になってきている。これらの閲覧規制の方法として、DNSポイズニングや、URLフィルタ等の方式があるが、オーバーブロッキングを防ぐためにはURLフィルタが必要である。本稿では、U …
NAID 110009545067

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