This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ. Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate. Download your certificate at: http://www.sigma-aldrich.com.
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Legal Information
TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
In the present work, a facile one-pot method is designed to fabricate a core-shell fluorescent nanoparticle (NP) for cellular imaging based on a new cationic conjugated polymer, poly[9,9'-bis(6,6'-(N,N,N-trimethylaminium)fluorene-2,7-ylenevinylene-co-alt-2,5-dicyano-1,4-phenylene] (PFVCN). Gold nanoflowers (AuNFs) are prepared by a seedless method, in which
Polycyclic aromatic hydrocarbons (PAHs) are of great environmental and human health concerns due to their widespread occurrence, persistence and carcinogenic properties. There is now compelling evidence that the mangrove sediment microbial structure is susceptible to PAHs contamination. The study aimed
Journal of nanoscience and nanotechnology, 13(7), 5194-5202 (2013-08-02)
Organic nanowires based on a fluorene homopolymer and a copolymer, i.e., poly(9,9-dioctylfluorene), F8, and poly(9,9-dioctylfluorene-co-benzothiadiazole), F8BT, respectively, were synthesised by solution assisted wetting of porous anodic alumina templates. Nanowires ranged between 3 microm and 50 microm in length, and were
Philosophical transactions. Series A, Mathematical, physical, and engineering sciences, 370(1972), 3787-3801 (2012-07-04)
We have investigated the energy transfer dynamics in a supramolecular linear polymer chain comprising oligofluorene (OF) energy donor units linked by quadruple hydrogen-bonding groups, and oligophenylene (OPV) chain ends that act as energy acceptors. Using femtosecond spectroscopy, we followed the
The Journal of organic chemistry, 78(17), 8789-8795 (2013-08-15)
Diphenylcarbene (DPC) generated by high-intensity laser photolysis of diphenyldiazomethane rearranges to fluorene (FL) by two distinct mechanisms as revealed by methyl-group labeling. Thus, excimer laser irradiation of p,p'-dimethyldiphenyldiazomethane generates 3,6-dimethylfluorene (3,6-DMF) and 2,7-dimethylfluorene (2,7-DMF), which were identified by fluorescence measurements
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