On-resin analysis

On-resin analysis is analysis of compound attached to a polymeric carrier material. 

The power of the HR-MAS method for on-resin analysis has been further underscored in the development of new linkers. Without this method, only indirect analytical data after removal from the resin was available. Direct assessment of the resin-bound linker greatly facilitated the introduction of a 4,5-dibromo octane- 1,8-diol linker that was converted into an octane-1,8-diol linker cleavable by olefin metathesis at the end of the synthesis.6 The disappearance and reappearance of the olefinic protons as well as the growing oligosaccharide chain was clearly visible in the H spectrum (Fig. 8.7).7... 

To determine if a solid-phase reaction is complete, on-resin analytical methods are preferable [6]. First, the quantitative or qualitative information obtained from on-resin analysis is more relevant to solid-phase reactions. Secondly, this kind of analysis is fast, direct, and without any alteration to the sample. On the other hand, analysis after cleavage would depend on the cleavage efficiency (to be discussed later) and the stability of analyte to cleavage conditions such as TFA. The... 

The effectiveness of the glycal assembly approach to solid support oligosaccharide synthesis was impressively documented by on-resin analysis. The crude product of the multistep synthesis of trisaccharide 32 (Scheme 16) was monitored by high-resolution magic angle spinning NMR (HR-MAS) [70]. 

For on-bead analysis vibrational spectroscopy (IR-spectroscopy) can be employed attenuated total reflection is a method allowing fast and nondestructive on-bead analysis of small samples (single bead analysis) without significant sample preparation. Solid phase NMR is the method of choice if complex structural analysis is intended on the support. Spatially resolved analysis on the resin is possible with microscopic techniques. 

TXRF is frequently used for contamination control and ultrasensitive chemical analysis, in particular in relation to materials used in semiconductor manufacturing [278,279], and metallic impurities on resin surfaces, as in PFA sheets [279,280], TXRF has been used by Simmross et al. [281] for the quantitative determination of cadmium in the four IRMM polyethylene reference materials (VDA-001 to 004). Microsamples (20-100 ig) from each reference material were transferred by hot pressing at 130 °C as 3 xm thin films straight on to quartz glass discs commonly used for TXRF analysis. The results obtained were quite satisfactory (Table 8.50). Other reports of the forensic application to plastic materials by TXRF have appeared [282], including a study of PE films by elemental analysis [283],... 

In 2001, Sarko and coworkers disclosed the synthesis of an 800-membered solution-phase library of substituted prolines based on multicomponent chemistry (Scheme 6.187) [349]. The process involved microwave irradiation of an a-amino ester with 1.1 equivalents of an aldehyde in 1,2-dichloroethane or N,N-dimethyl-formamide at 180 °C for 2 min. After cooling, 0.8 equivalents of a maleimide dipo-larophile was added to the solution of the imine, and the mixture was subjected to microwave irradiation at 180 °C for a further 5 min. This produced the desired products in good yields and purities, as determined by HPLC, after scavenging excess aldehyde with polymer-supported sulfonylhydrazide resin. Analysis of each compound by LC-MS verified its purity and identity, thus indicating that a high quality library had been produced. 

The bromination reaction (Scheme 12.3) was also carried out on resins (1) of three different sizes (Fig. 12.5). Single bead FTIR study and the kinetics analysis were carried out as in the esterification reaction studies. Rate constants are hsted in Tab. 12.2. The relationship between the rate constants and the bead size is shown in Fig. 12.7b. 

In a dehydration reaction (Scheme 12.4), the IR band of the formamide carbonyl group at 1684 cm in (7) decreased and eventually converted to the isonitrile band at 2150 cm in (8) (Fig. 12.8). In a separate example (Scheme 12.5), the conversion of the IR band from the carbonate carbonyl group in (9) to the IR band of the carbamide carbonyl group in (10) can be monitored to assure the reaction completion (Fig. 12.9). Based on FTIR analysis, the reaction time course can be analyzed by integrating peak areas of the IR bands from the starting resin and the product. From the point of view of kinetics, the side reaction product formation can be excluded if the pseudo first order rates of the starting material consumption and the product formation are identical. 

Resin Analysis. Thermal analysis of the BCB resin systems included Differential Scanning Calorisietry (DSC) using a DuPont 010 cell and Thermal Gravimetric Analysis (TGA) run on a DuPont 951 TGA, the entire thermal analysis system run using an Omnitherm model 35053... 

Separation of carbon tetrachloride from biological samples may achieved by headspace analysis, purge-and-trap collection from aqueous solution or slurry samples, solvent extraction, or direct collection on resins. Headspace analysis offers speed, simplicity, and good reproducibility, but partitioning of the analyte between the headspace and the sample matrix is dependent upon the nature of the matrix and must be determined separately for each different kind of matrix (Walters 1986). 

The analysis of the reported source countries (ARQ, 2002-2006 period) suggests that cannabis resin production takes place in some 58 countries while cannabis herb (marijuana) production occurs in at least 116 countries. The caveat here is that cannabis herb is thought to be produced even in countries where the main supply concentrates on resin. Cannabis herb production is globally far more dispersed than global cannabis resin production. 

In a similar way, Guiles and co-workers immobilized an aryl pinacol boronate on resin via an ester linkage, and then a small number of aryl halides were coupled to this (Scheme 31). The products were cleaved and immediately transformed into their methyl esters, presumably for ease of analysis and separation from unreacted boronate. The reaction was found to be slower than that of the opposite polarity (i.e., with the resin-bound iodide), and only moderate yields were obtained after as much as 48 h. Yields could be considerably improved upon a second round of coupling, but only one example was given of this. The aryl bromides were found to react only upon heating. 

The above described methodology was found to be very useful in a solid-supported synthesis of pyrazoles and pyrimidines via propenones developed by Westman and co-workers35 (Scheme 5.19). Merrifield resin was reacted with methylamine in water at 150°C for 10 min to form the solid-supported benzylmethylamine (3) in high yield (86% yield, 1.08 mmol/g based on elemental analysis). After washing, the resin was treated with 5 equiv. DMFDEA and 5 equiv of 4-phenoxyacetophenone at 180°C for 10 min in DMF to form the solid supported benzyl methyl aminopropenones (4). 

At higher temperatures, a broad transition, present in all epoxy resins independently of the reacting species (amines or anhydrides), is much more complex than the y transition. Its position and shape vary strongly with the chemical structure of the epoxy resin. The dynamic mechanical response and the solid-state 13C NMR of the various model networks referred to in Table 9 focus precisely on the analysis of this /3 transition [62,63]. 

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