Ultrafast Conversions of Hydrogen-Bonded Structures in Liquid Water Observed via Femtosecond Soft X-ray Spectroscopy

Author(s):  
N. Huse ◽  
H. Wen ◽  
H. Cho ◽  
T.-K. Kim ◽  
R.W. Schoenlein ◽  
...  
Keyword(s):  
X Ray ◽  
2009 ◽  
Vol 131 (23) ◽  
pp. 234505 ◽  
Author(s):  
Haidan Wen ◽  
Nils Huse ◽  
Robert W. Schoenlein ◽  
Aaron M. Lindenberg
Keyword(s):  
X Ray ◽  

2019 ◽  
Author(s):  
KAIKAI MA ◽  
Peng Li ◽  
John Xin ◽  
Yongwei Chen ◽  
Zhijie Chen ◽  
...  

Creating crystalline porous materials with large pores is typically challenging due to undesired interpen-etration, staggered stacking, or weakened framework stability. Here, we report a pore size expansion strategy by self-recognizing π-π stacking interactions in a series of two-dimensional (2D) hydrogen–bonded organic frameworks (HOFs), HOF-10x (x=0,1,2), self-assembled from pyrene-based tectons with systematic elongation of π-conjugated molecular arms. This strategy successfully avoids interpene-tration or staggered stacking and expands the pore size of HOF materials to access mesoporous HOF-102, which features a surface area of ~ 2,500 m2/g and the largest pore volume (1.3 cm3/g) to date among all reported HOFs. More importantly, HOF-102 shows significantly enhanced thermal and chemical stability as evidenced by powder x-ray diffraction and N2 isotherms after treatments in chal-lenging conditions. Such stability enables the adsorption of dyes and cytochrome c from aqueous media by HOF-102 and affords a processible HOF-102/fiber composite for the efficient photochemical detox-ification of a mustard gas simulant.


2021 ◽  
Vol 12 (16) ◽  
pp. 3996-4002
Author(s):  
Vinícius Wilian D. Cruzeiro ◽  
Andrew Wildman ◽  
Xiaosong Li ◽  
Francesco Paesani

Polyhedron ◽  
2005 ◽  
Vol 24 (8) ◽  
pp. 865-871 ◽  
Author(s):  
Mohan S. Bharara ◽  
Chong H. Kim ◽  
Sean Parkin ◽  
David A. Atwood

1987 ◽  
Vol 40 (7) ◽  
pp. 1147 ◽  
Author(s):  
EJ Oreilly ◽  
G Smith ◽  
CHL Kennard ◽  
TCW Mak

The crystal structures of (2-formyl-6-methoxyphenoxy)acetic acid (1), diaquabis [(2-formyl-6-methoxyphenoxy) acetato ]zinc(11) (2), tetraaquabis [(2-chlorophenoxy) acetato ]zinc(11) (3), triaquabis [(2-chlorophenoxy) acetato ]cadmium(11) dihydrate (4) and lithium (2-chloro- phenoxy )acetate 1.5 hydrate (5) have been determined by X-ray diffraction. The acid (1) forms centrosymmetric hydrogen-bonded cyclic dimers [O…0, 2.677(6) �] which are non-planar. Complex (2) is six-coordinate with two waters [Zn- Ow , 1.997(2) �] and four oxygens from two asymmetric bidentate carboxyl groups [Zn-O, 2.073, 2.381(2) �] completing a skew trapezoidal bipyramidal stereochemistry. Complex (5) is also six-coordinate but is octahedral, with two trans-related unidentate carboxyl oxygens [mean Zn-O, 2.134(9) �] and four waters [mean Zn-O, 2.081(9) �]. The seven-coordinate complex (4) has crystallographic twofold rotational symmetry relating two :symmetric bidentate acid ligands [ Cd -O, 2.26, 2 48(:) �] and two waters [ Cd -O, 2.34(2) �] while the third water lies on this axis [ Cd -O, 2.27(2) �]. In contrast to the monomers (2)-(4), complex (5) is polymeric with tetrahedral lithium coordinated to one water and three carboxylate oxygens [mean Li-0, 1.95(1) �]. The essential conformation of the free acid is retained in complexes (2), (3) and (4) but in (5), it is considerably changed.


2021 ◽  
Vol 507 ◽  
pp. 230285
Author(s):  
Hiroshi Naito ◽  
Kenta Ishikawa ◽  
Takashi Sasabe ◽  
Shuichiro Hirai ◽  
Toshihiro Tanuma

CrystEngComm ◽  
2021 ◽  
Author(s):  
Mger A. Navasardyan ◽  
Stanislav Bezzubov ◽  
Alexander G. Medvedev ◽  
Petr V Prikhodchenko ◽  
Churakov Andrei

Novel peroxosolvates of tetraalkylammonium halides Et4N+Cl–•2(H2O2) (1), Et4N+Br–•2(H2O2) (2), Me3(ClCH2CH2)N+Cl–•H2O2 (3) and Me3PhN+Cl–•H2O2 (4) were prepared from concentrated hydrogen peroxide and the corresponding structures were determined by X-ray crystallography. Structures...


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