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The self-assembly of a series of 1,3-disubstituted benzenes has been scrutinized by scanning tunneling microscopy (STM) and computational modeling. Small changes in the functional groups (e.g., ester, thioester, ketone) resulted in dramatic changes in packing patterns. Remarkably, several of the molecules gave rise to monolayers with more than one molecule in the asymmetric unit and displayed multiple packing patterns. This constitutes the most complex behavior observed to date in this type of monolayer and illuminates several issues of importance in three-dimensional crystallization. Intermolecular interactions associated with the observation of multiple molecules in the asymmetric unit and stabilization of pseudopolymorphs were identified. The geometry and electrostatic properties of the isolated molecule and monolayer density were found to be critical in determining which packing motif was adopted. 相似文献
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Synthesis, Crystal Structure, Electronic Structure, Spectroscopic and Magnetic Properties of [VOCl2{P(SiMe3)3}2]: A Phosphane Complex with a Disordered VOCl2 Group VOCl3 reacts with P(SiMe3)3 to form blue green crystals of [VOCl2{P(SiMe3)3}2] ( 1 ). The X-ray crystal structure analysis of 1 (cubic space group P213: a = 1541.4(1) pm, Z = 4) reveals a slightly distorded trigonal bipyramidal coordination environment for the disordered vanadium(IV) center. Density functional calculations on the compound [VOCl2{P(SiH3)3}2] ( 2 ) are in accord with this observation. 1 has been characterized by ESR, vibrational (IR and Raman) and electronic absorption spectroscopy and magnetic measurements. The ESR spectra of 1 in a toluene solution (293 K and frozen solution at 6 K) exhibit hyperfine interactions of the unpaired electron with the 51V center (I = 7/2) and the 31P centers (I = 1/2) of the two equivalent phosphane ligands. The ligand-field transitions of the VOCl2{P}2 chromophore observed in the electronic absorption spectrum have been assigned on the basis of density functional calculations on 2 . 相似文献
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Synthesis and Structure of a Binuclear Gadolinium(III) Complex: Magnetic Exchange Interactions in Alkoxy Bridged Lanthanide Complexes The Schiff Base ligand N-salicylidene-2-(bis-(2-hydroxyethyl)amino)ethylamine (H3sabhea) reacts with Gd(NO3)3 · 6 H2O in methanol solution to yield the alkoxy bridged binuclear gadolinium(III) complex [{Gd(Hsabhea)(NO3)}2] · 2MeOH ( 1 ). 1 crystallizes in the monoclinic space group P21/c with a = 1014.8(2), b = 2059.2(4), c = 867.5(2) pm, β = 106.72(2)°, and Z = 2. The two gadolinium atoms are bridged by two alkoxide oxygen atoms with angles of 107.60(11)° at the oxygen bridgeheads and a Gd? Gd separation of 376.43(7) pm. A variable-temperature magnetic susceptibility study (2 to 280 K) of 1 revealed an antiferromagnetic coupling between the Gd(III) ions with J = ?0.198 cm?1 (g = 1.975). 相似文献
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Handzy DO Bauer W Daffin FC Gaff SJ Gelbke CK Glasmacher T Gualtieri E Hannuschke S Huang MJ Kunde GJ Lacey R Li T Lisa MA Llope WJ Lynch WG Martin L Montoya CP Pak R Peaslee GF Pratt S Schwarz C Stone N Tsang MB Vander Molen AM Westfall GD Yee J Yennello SJ 《Physical review letters》1995,75(16):2916-2919
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M. Winkler B. Achenbach K.-H. Behr M. Berz D. Boutin C. Brandau H. Emling H. Geissel H. Iwase C. Karagiannis A. Kelic H. Leibrock Y. Litvinov S. Manikonda J. A. Maruhn G. Moritz C. Mühle G. Münzenberg C. Nociforo W. Plass C. Scheidenberger H. Simon K. Sümmerer M. Svedentsov N. A. Tahir A. Tauschwitz Z. Wang H. Weick H. Wollnik M. Yavor 《The European physical journal. Special topics》2007,150(1):263-264
The Super-FRS will be a large-acceptance two-stage superconducting fragment separator with three exit branches serving different
experimental areas. Due to the high primary-beam intensity of up to 1012 ions/s a challenging design of the target area and the components used in the first dipole
Super-FRS is necessary. These efforts include high-power production targets, beam-dumps to catch the remaining primary beam,
and radiation resistant magnets. In this contribution we summarize the recent developments on these issues. 相似文献
129.
L.M. Zambov C. Popov M.F. Plass A. Bock M. Jelinek J. Lancok K. Masseli W. Kulisch 《Applied Physics A: Materials Science & Processing》2000,70(5):603-606
The humidity sensitive properties of carbon nitride (CNx) films deposited by two methods, inductively coupled plasma chemical vapour deposition utilizing transport reactions and
pulsed laser deposition combined with an rf discharge, have been investigated. For this purpose capacitance humidity sensors
with a CNx detecting element have been fabricated and tested. Fast and significant responses toward moisture are registered by the changes
of the electrical parameters. The CNx films sensing mechanism has been discussed. The results obtained show unambiguously that CNx films appear to be a promising candidate as a humidity sensitive element in up-to-date electronic noses.
Received: 6 December 1999 / Accepted: 7 January 2000 / Published online: 24 March 2000 相似文献
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