Conjugate base-sensitive

The l"-and 2"-hydroxy derivatives which were reported by Burstein et al. (13) and shown in Figure 4. These were found in raEbit urine and appeared to be present as base-sensitive conjugates. 

Note 1. No cyanide was used to remove the copper salts, since the nitrile is probably very base-sensitive (isomerization to a conjugated diene). 

The aim of this chapter is to give a state-of-the-art report on the plastic solar cells based on conjugated polymers. Results from other organic solar cells like pristine fullerene cells [7, 8], dye-sensitized liquid electrolyte [9], or solid state polymer electrolyte cells [10], pure dye cells [11, 12], or small molecule cells [13], mostly based on heterojunctions between phthaocyanines and perylenes [14], will not be discussed. Extensive literature exists on the fabrication of solar cells based on small molecular dyes with donor-acceptor systems (see for example [2, 3] and references therein). 

Acid- and base-sensitive lipidated peptides can be selectively deprotected by enzymatic hydrolysis of choline esters.[13al Choline esters of simple peptides, but also of sensitive peptide conjugates like phos-phorylated and glycosylated peptides,1141 nucleopep-tides1151 and lipidated peptides,113,1631 can be cleaved with acetyl choline esterase (AChE) and butyryl choline esterase (BChE) under virtually neutral conditions with complete chemoselectivity. Acid-labile farnesyl groups and base-sensitive thioesters are not attacked. 

Unfortunately, several important classes of a-diazo ketones cannot be prepared in good yield via these standard methods. a -Diazo derivatives of a.p-unsaturated ketones, for example, have previously proved to be particularly difficult to prepare.1113 12 The acylation of diazomethane with a.p-unsaturated acid chlorides and anhydrides is generally not a successful reaction because of the facility of dipolar cycloaddition to conjugated double bonds, which leads in this case to the formation of mixtures of isomeric pyrazolines. Also problematic are diazo transfer reactions involving base-sensitive substrates such as certain a,p-enones and heteroaryl ketones. Finally, the relatively harsh conditions and lack of regioselectivity associated with the thermodynamically controlled Claisen formylation step in the "deformylative" diazo transfer procedure limit the utility of this method when applied to the synthesis of diazo derivatives of many enones and unsymmetrical saturated ketones. 

A sharp blue-to-red color change was observed with Poly- -Glu-Bis-3 upon the increase of pH. As expected, the existence of multiple base-sensitive carboxylic acid residues in the molecule resulted in a chromatic transition at a lower pH region compared to the poly-I-Glu-PDA assemblies discussed earlier. At pH 7.5, the blue polymer turned completely red as a result of significantly shortened conjugation length induced by the side chain disorder arising from increased electrostatic repulsion between deprotonated surface carboxylates. 

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