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A refined crystal structure of andrographolide has been obtained by X-ray anaysis using CuKα radiation. It crystallizes in the monoclinic crystal system with unique b-axis in space group P21. The unit cell parameters are a = 6.552(2) Å, b = 8.009(1) Å, c = 17.989(1) Å and interaxial angle β = 97.32(1)°. The structure has been solved by direct methods and was refined up to R = 0.041, ωR = 0.0464. Both the cyclohexane rings are in chair conformation with the furan ring in twist conformation. The crystal structure is stabilized by hydrogen bonding. 相似文献
785.
Varsha Lisa John A. R. Nayana T. R. Keerthi Athira Krishnan K. A. B. C. P. Sasidharan Vinod T. P. 《Macromolecular bioscience》2023,23(9):2300081
Silk fibers (SF) reeled from silkworms are constituted by natural proteins, and their characteristic structural features render them applicable as materials for textiles and packaging. Modification of SF with functional materials can facilitate their applications in additional areas. In this work, the preparation of functional SF embedded with carbon dots (CD) is reported through the direct feeding of a CD-modified diet to silkworms. Fluorescent and mechanically robust SF are obtained from silkworms (Bombyx mori) that are fed on CDs synthesized from the Morus rubra variant of mulberry leaves (MB-CDs). MB-CDs are introduced to silkworms from the third instar by spraying them on the silkworm feed, the mulberry leaves. MB-CDs are synthesized hydrothermally without adding surface passivating agents and are observed to have a quantum yield of 22%. With sizes of ≈4 nm, MB-CDs exhibited blue fluorescence, and they can be used as efficient fluorophores to detect Dopamine (DA) up to the limit of 4.39 nM. The nanostructures and physical characteristics of SF weren't altered when the SF are infused with MB-CDs. Also, a novel DA sensing application based on fluorescence with the MB-CD incorporated SF is demonstrated. 相似文献
786.
We have found that the specific rate of α‐sulfonyl carbanion formation in a β‐substituted sulfone shows a sizable dependence on the H Cα Cβ X torsion angle. Defining kN = (kexch)X/(kexch)model (where the model has X = H or an alkyl group) we observed for a collection of β‐alkoxy sulfones (X = OR) acceptable agreement with the expression log kN = a + b cos2 θ (where a = 1.70 and b = 2.62). Extension to other β‐substituents (X = RS, R2N, and R3N+) yields the same pattern, with the last showing very large dependence of kN on the torsion angle (b = 6.3). These observations are ascribed to the presence (in addition to the inductive and field effects) of negative hyperconjugation responsible for accelerations of 1000‐fold and more, deriving from donation of the incipient negative charge on carbon into the σ*C X orbital in the transition state. These observations reflect, and at the same time underline, the importance of the low‐lying antibonding orbitals present in heteroatomic molecules. © 2002 Wiley Periodicals, Inc. Heteroatom Chem 13:397–405, 2002; Published online in Wiley Interscience (www.interscience.wiley.com). DOI 10.1002/hc.10067 相似文献
787.
Vandana Jaiswal Soumik Mondal Bandana Singh Prof. Vinod. P. Singh Prof. Dr. Jaideep Saha 《Angewandte Chemie (International ed. in English)》2023,62(30):e202304471
Access to 1,3-functionalized azetidines through a diversity-oriented approach is highly sought-after for finding new applications in drug-discovery. To this goal, strain-release-driven functionalization of azabicyclo[1.1.0]-butane (ABB) has generated significant interest. Through appropriate N-activation, C3-substituted ABBs are shown to render tandem N/C3-fucntionalization/rearrangement, furnishing azetidines; although, modalities of such N-activation vis-à-vis N-functionalization remain limited to selected electrophiles. This work showcases a versatile cation-driven activation strategy of ABBs. And capitalizes on the use of Csp3 precursors amenable to forming reactive (aza)oxyallyl cations in situ. Herein, N-activation leads to formation of a congested C−N bond, and effective C3 activation. The concept was extended to formal [3+2] annulations involving (aza)oxyallyl cations and ABBs, leading to bridged bicyclic azetidines. Besides the fundamental appeal of this new activation paradigm, operational simplicity and remarkable diversity should engender its prompt use in synthetic and medicinal chemistry. 相似文献