Results 21 to 30 of about 249,594 (250)

1-[1,4-Bis(but-3-en-1-yloxy)]-2,3,4,5-(1,4-dimethoxy)pillar[5]arene–1,4-dibromobutane 1:1 inclusion complex

open access: yesIUCrData, 2023
In the title compound, C51H58O10·C4H8Br2, both the host and guest are completed by crystallographic twofold symmetry (one carbon atom of the host lies on the rotation axis).
Mickey Vinodh, Talal F. Al-Azemi
doaj   +1 more source

Reinforced molecular recognition as an alternative to rigid receptors [PDF]

open access: yes, 2006
In theory, a perfectly rigid receptor will probably be an unbeatable binder. However, rigidity may not be easy to achieve in practice and it is certainly not Nature’s method to realise high affinity. In many proteins binding affinity is increased through
Otto, Sijbren,
core   +1 more source

Host-Guest Complexations of Amine Boranes and Isoelectronic/Isostructural Quaternary Alkylammonium Cations by Cucurbit[7]uril in Aqueous Solution

open access: yesHeteroatom Chemistry, 2019
The host-guest complexation of six amine boranes (R3NBH3) by the macrocyclic host molecule cucurbit[7]uril (CB[7]) in aqueous solution has been investigated using 1H and 11B NMR spectroscopy.
Mona A. Gamal-Eldin, Donal H. Macartney
doaj   +1 more source

9,9′-(Biphenyl-2,2′-diyl)difluoren-9-ol 4-methylpyridine solvate

open access: yesActa Crystallographica Section E, 2010
The title compound, C38H26O2·C6H7N, crystallized as a host–guest complex from a solvent mixture of 4-methylpyridine and acetone. The dihedral angle between the rings in the biphenyl unit is 87.06 (3)°.
Jamshid Ashurov   +3 more
doaj   +1 more source

Quantification of Solvent Contribution to the Stability of Noncovalent Complexes [PDF]

open access: yes, 2013
We introduce an indirect approach to estimate the solvation contributions to the thermodynamics of noncovalent complex formation through molecular dynamics simulation.
Hetényi, Csaba   +3 more
core   +1 more source

An Operative Electrostatic Slipping Mechanism along Macrocycle Flexibility Accelerates Guest Sliding during pseudo‐Rotaxane Formation

open access: yesChemistryOpen, 2022
A pseudo‐rotaxane is a host−guest complex composed of a linear molecule encircled by a macrocyclic ring. These complexes can be assembled by sliding the host over the guest terminal groups.
Dr. Aldo C. Catalán   +3 more
doaj   +1 more source

Cyclodextrin Inclusion Complexes with Antibiotics and Antibacterial Agents as Drug-Delivery Systems—A Pharmaceutical Perspective

open access: yesPharmaceutics, 2022
Cyclodextrins (CDs) are a family of cyclic oligosaccharides, consisting of a macrocyclic ring of glucose subunits linked by α-1,4 glycosidic bonds. The shape of CD molecules is similar to a truncated cone with a hydrophobic inner cavity and a hydrophilic
Dariusz Boczar, Katarzyna Michalska
doaj   +1 more source

Study of the Counter Anions in the Host-Guest Chemistry of Cucurbit[8]uril and 1-Ethyl-1′-benzyl-4,4′-bipyridinium

open access: yesThe Scientific World Journal, 2013
A series of 1-ethyl-1′-benzyl-4,4′-bipyridinium compounds with different counter anions (BEV-X2, where the X is Cl, Br, I, PF6, ClO4) were synthesized.
Hailong Ji, Fengyu Liu, Shiguo Sun
doaj   +1 more source

Supramolecular polymer hydrogels induced by host-guest interactions with di-[cyclobis(paraquat-p-phenylene)] cross-linkers: from molecular complexation to viscoelastic properties [PDF]

open access: yes, 2017
Supramolecular polymer networks have been designed on the basis of a -electron donor/acceptor complex: naphthalene (N)/cyclobis(paraquat-p-phenylene) (CBPQT4+=B). For this purpose, a copolymer of N,N-dimethylacrylamide P(DMA-N1), lightly decorated with 1
Belal, Khaled   +7 more
core   +3 more sources

Complexation of enalapril maleate with beta-cyclodextrin: NMR spectroscopic study in solution</a> </p><span class="r_subtitle"><img src="/img/openaccess.ico" alt="open access: yes" title="open access: yes" width="16" height="16"><i>Química Nova</i>, 2006 </span><br><span class="r_content">A detailed NMR (¹H , COSY, ROESY) spectroscopic study of complexation of enalapril maleate with beta-cyclodextrin was carried out. The ¹H NMR spectrum of enalapril maleate confirmed the existence of cis-trans equilibrium in solution, possibly due to ...</span><br><span class="r_sub"><i>Syed Mashhood Ali<span id="ma_10" style="display:none">, Arti Maheshwari, Fahmeena Asmat, Mamoru Koketsu</span>   <small><a href="#" style="color:#808080;" onClick="return toggle_div(this, 'ma_10')">+3 more</a></small></i></span><br><small><a href="https://doaj.org/article/40eabe9ee075492cb645bcff76a0b374" target="_blank" rel="nofollow" title="doaj.org/article/40eabe9ee075492cb645bcff76a0b374">doaj</a> </small>   <div id="more_10" style="display:none"><a href="/sci_redir.php?doi=10.1590%2FS0100-40422006000400011" target="_blank" rel="nofollow">openaccessbutton.org (pdf)</a><br><a href="javascript:navigator.clipboard.writeText('10.1590/S0100-40422006000400011'); alert('Copied the doi');">copy doi</a> <small>(10.1590/S0100-40422006000400011)</small><br></div><small><a href="#" onClick="return toggle_div(this, 'more_10')">+1 more source</a></small><br></div><div class="r"><div style="margin-bottom:2px;overflow:hidden"><div style="display: inline-block; float: left; font-size: small; padding-right: 16px; margin-top: -1px; padding-bottom: 1px;"><a href="/q-inclusion_complex/" class="suggestion"onclick="show_loader();"><b>inclusion complex</b></a><br/><a href="/q-crystal_structure/" class="suggestion"onclick="show_loader();"><b>crystal structure</b></a><br/><a href="/q-science/" class="suggestion"onclick="show_loader();"><b>science</b></a><br/></div><div style="display: inline-block; float: left; font-size: small; padding-right: 16px; margin-top: -1px; padding-bottom: 1px;"><a href="/q-medicine/" class="suggestion"onclick="show_loader();"><b>medicine</b></a><br/><a href="/q-cyclodextrin/" class="suggestion"onclick="show_loader();"><b>cyclodextrin</b></a><br/><a href="/q-host-guest_complex/" class="suggestion"onclick="show_loader();"><b>host-guest complex</b></a><br/></div><div style="display: inline-block; float: left; font-size: small; padding-right: 16px; margin-top: -1px; padding-bottom: 1px;"><a href="/q-molecular_recognition/" class="suggestion"onclick="show_loader();"><b>molecular recognition</b></a><br/></div></div></div><div class="pagenav"><a href="/q-host%E2%80%93guest_complex/p-2/" rel="nofollow"><b>previous</b></a>   <a href="/q-host%E2%80%93guest_complex/" rel="nofollow">1</a>  <a href="/q-host%E2%80%93guest_complex/p-2/" rel="nofollow">2</a>  <b>3</b>  <a href="/q-host%E2%80%93guest_complex/p-4/" rel="nofollow">4</a>  <a href="/q-host%E2%80%93guest_complex/p-5/" rel="nofollow">5</a>   <a href="/q-host%E2%80%93guest_complex/p-4/" id="next" rel="nofollow"><b>next</b></a> </div><br></div> </div> <script>document.getElementById('loadingGif').style.display='none';</script><div style="width: 100%; height: 40px; bottom: 0px; background-color: #f5f5f5;"><div style="padding-left: 15px; padding-top: 10px"> <a href="/" rel="nofollow">Home</a> - <a href="/page-about/" rel="nofollow">About</a> - <a href="/page-disclaimer/" rel="nofollow">Disclaimer</a> - <a href="/page-privacy/" rel="nofollow">Privacy</a> </div></div> <link rel="stylesheet" href="//ajax.googleapis.com/ajax/libs/jqueryui/1.11.4/themes/smoothness/jquery-ui.min.css"/> </body> </html>