dc.contributor.author
Cera, Luca
dc.contributor.author
Schalley, Christoph A.
dc.date.accessioned
2018-06-08T03:37:49Z
dc.date.available
2014-10-22T07:20:22.304Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/15593
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-19781
dc.description.abstract
A six-station linear guest for cucurbit[7]uril and cucurbit[8]uril has been
synthesized in order to implement a cascade of transformations driven by
external stimuli. The guest chain is sequence-programmed with electron-
deficient viologen and electron-rich naphthalene stations linked by either
flexible or rigid spacers that affect the chain's folding properties. Together
with the orthogonal guest selectivity of the two cucurbiturils, these
properties result in self-sorted cucurbituril pseudorotaxane foldamers. Each
transformation is controlled by suitable chemical and redox inputs and leads
not only to refolding of the guest chain, but also to the liberation of
secondary messenger molecules which render the system presented here
reminiscent of natural signaling cascades. The steps of the cascade are
analyzed by UV/Vis, 1H NMR and electrospray (tandem) mass spectrometry to
investigate the different pseudorotaxane structures in detail. With one guest
oligomer, three different cucurbiturils, and several different chemical and
redox inputs, a chemical system is created which exhibits complex behavior
beyond the chemist's paradigm of the pure chemical compound.
en
dc.rights.uri
http://creativecommons.org/licenses/by-nc/3.0/
dc.subject.ddc
500 Naturwissenschaften und Mathematik::540 Chemie
dc.title
Stimuli-induced folding cascade of a linear oligomeric guest chain programmed
through cucurbit[n]uril self-sorting (n = 6, 7, 8)
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Chemical Science. - 5 (2014), 6, S. 2560-2567
dc.identifier.sepid
35780
dcterms.bibliographicCitation.doi
10.1039/C3SC53211A
dcterms.bibliographicCitation.url
http://xlink.rsc.org/?DOI=C3SC53211A
refubium.affiliation
Biologie, Chemie, Pharmazie
de
refubium.funding
OpenAccess Publikation in Allianzlizenz
refubium.funding.id
Au-006328
refubium.mycore.fudocsId
FUDOCS_document_000000021187
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000004078
dcterms.accessRights.openaire
open access
dcterms.isPartOf.issn
2041-6520