LETTUCE SEED GERMINATION: EFFECTS OF HIGH TEMPERATURE AND OF REPEATED FAR-RED TREATMENT IN RELATION TO PHYTOCHROME

Abstract— At 37°C the active form of phytochrome in lettuce seed cannot function to promote subsequent germination. This effect of high temperature is distinct from thermal acceleration of dark reversion from the active form of phytochrome to the inactive form, and may be due to reversible denaturation of phytochrome.
Repeated brief irradiations with far-red light inhibit subsequent germination in the whole seed, whereas a similar irradiation regime results in a strong enhancement of the development of growth potential (ability to expand against an externally-imposed osmotic restraint) in the excised axial portion of the seed. A possible explanation for these two opposing results, in volving two different pigment systems with effective loci in different parts of the seed, is suggested.     

Radiation-induced grafting of hexafluoroacetone to polyethylene

Although hexafluoroacetone is not polymerized by ionizing radiation, it is shown that γ-irradiation of hexafluoroacetone dissolved in polyethylene films produces a graft with a G value of 500 and, therefore, a kinetic chain length of 200. The effects of dose rate (0.021–3.55 Mrad/hr), temperature (21–53°C), and pressure (1.5–6.2 atm) on the graft rates have been measured. Also the effect of temperature (21–53°C) on the postirradiation grafting reaction and on the physical properties of the grafted films have been investigated. Together with solubility, diffusivity, infrared, and EPR data, the results lead to the following mechanism: The first step represents production of secondary alkyl radicals in the polyethylene by irradiation of the polymer–monomer system. The second step involves the linkage of the monomer to the radical site to form the alkoxy radical. Since it cannot add to another monomer unit, this radical abstracts a hydrogen atom from an adjacent polyethylene chain in the third step. Radical R· can then continue the kinetic chain. Radical combination and radical–impurity reactions terminate the chain. The graft may be unique in that it is the only one we have found in which a pendant group containing only one monomer unit is attached by a chain reaction. At dose rates up to 0.215 Mrad/hr, the grafting was linear with time and proportional to the 0.73 power of the dose rate at 21°C and to the 0.81 power at 53°C. The reaction is insensitive to increases in dose rate above 0.215 Mrad/hr where diffusivity measurements show the reaction to be diffusion-controlled. The rate of reaction increased 10% when the temperature was increased from 21 to 53°C. While there was significant postirradiation grafting reaction at 21°C, there was none at 53°C. The results do not fit the equations of reaction-controlled steady-state graft-polymerization kinetics. The deviations arise from an observed increase in monomer solubility in the film with increasing graft combined with low diffusivity of the monomer in polyethylene, and the presence of a radical-scavenging impurity which terminates the kinetic chain with the appearance of a relatively stable radical. EPR data suggests that the impurity is a trace of oxygen which may be produced radiolytically.     

Cyclization of methyl 6,7-epoxycitronellate to methylcyclopentane derivatives : Alkoxide induced conversion of γ-lactones to γ,δ-unsaturated acids

The reaction of sodium hydride or potassium t-butoxide with methyl epoxycitronellate (1) in dimethylformamide affords a mixture of cis,cis-puleganolide (2) and cis,trans-puleganolide (3) in high yield. When the cyclization is conducted at 110°, the isomeric 2-isopropenyl-5-methylcyclopentanecarboxylic acids (8a–d) become the major products. It is demonstrated that γ-lactones undergo alkoxide-induced elimination to afford γ,δ-unsaturated acids.     

Accelerated exchange in polyelectrolyte multilayers by "catalytic" polyvalent ion pairing

Self-exchange of isotopically labeled polycarboxylic acid within a polyelectrolyte multilayer proceeds to completion and is reversible. Similar exchange with poly(styrene sulfonate), which forms nonlabile polyelectrolyte complexes, is slow and irreversible but is facilitated by polyvalent ion pairing interventions of a third polyelectrolyte. This is an example of accelerated kinetics in "sticky" synthetic systems associated by nonspecific polyvalent interactions.     

Estimation of urinary diamines and polyamines by thin-layer chromatography

The dansylated derivatives of ammonia, 1.3-diaminopropane, 1,4-diaminobutane, 1,5-diaminopentane, spermidine, histamine, and spermine were separated by one ascending development in chloroform—triethylamine (5:1) on a 250-μm silica gel 60 plate. Putrescine, cadaverine, spermidine, and spermine in human urine were quantitated by a direct scan of the fluorescent intensity of the spots corresponding to these compounds. Higher amounts of spermidine and spermine were found in the urines of cancer patients compared to the values of these substances in normal urine.     

Functionalization of substituted 2-(1H)pyridones. II. Synthetic pathways to c-6 modified 3-cyano- and 3-carboxy-2-(1H)pyridones from a common precursor

Starting from readily available 1,2-dihydro-6-methyl-2-oxo-3-pyridinecarbonitrile, 1, viable synthetic pathways to a number of C-6 functionalized 1,2-dihydro-2-oxo-3-pyridinecarbonitriles and corresponding acids are presented. Through the utilization of dianion chemistry, the C-6 methyl substituent is selectively functionalized to three different oxidation levels.     

Mass-spectrometric studies on alkylated 6-thiopurines

6-Thiopurine and its N- or C-alkyl derivatives all form an [M – 1]-ion upon fragmentation. In the 7-alkyl derivatives, this ion represents the major component of the spectrum. This is ascribed to formation of a five-membered thiazoline-like ring. Similar ring formation stabilises the [M – 1]-ion in the 7-methyl derivatives of hypoxanthine, adenine and 6-selenopurine.     

Methyl displacements from cyclopentadienyl ring planes in sterically crowded (C5Me5)3M complexes

The displacements of the methyl substituents away from the metal and out of the cyclopentadienyl ring plane are compared in sterically crowded (C(5)Me(5))(3)M complexes vs sterically normal f-element complexes in an attempt to evaluate the utility of this parameter in predicting unusual (C(5)Me(5))(1-) ring reactivity. The out-of-plane displacements of 16 sterically crowded tris(cyclopentadienyl) complexes of general formula (C(5)Me(5))(3)M, (C(5)Me(4)R)(3)M (R = Et, (i)Pr, (t)()Bu, SiMe(3)), (C(5)Me(5))(3)MX (X = anion), and (C(5)Me(5))(3)ML (L = neutral ligand) are compared with [(C(5)Me(5))(2)U](2)(C(6)H(6)), (C(5)Me(5))(2)Sm(PC(4)H(2)(t)Bu(2)), and 33 representative examples of f-element bis(cyclopentadienyl) complexes with normal cyclopentadienyl behavior and coordination numbers ranging from 6 to 10. In general, the methyl displacement values of sterically crowded complexes overlap with those in the other complexes, which demonstrates that the basis of the structural distortions is complex. However, if the most extreme out-of-plane displacement in each of the sterically crowded complexes is examined vs the analogous maximum out-of-plane displacement in less crowded systems, there appears to be a basis for predicting cyclopentadienyl reactivity.     

Trace Inequalities,Maximal Inequalities,and Weighted Fourier Transform Estimates

In the spirit of work of Kerman and Sawyer, a condition is given that is necessary and sufficient for the Fourier transform norm inequality $\Big(\int_{{\Bbb R}_d} \vert\hat{f}\vert^q d\mu\Big)^{1/q} \leq C\Big(\int_{{\Bbb R}_d} \vert f\vert^p v\Big)^{1/p}$ provided v is a radial weight for which v^?1/p is convexly decreasing and μ is a suitable measure. We also establish alternative conditions for such inequalities by proving corresponding trace type inequalities and maximal function inequalities that underlie the Fourier transform estimates. Our conditions are relatively simple to compute. Among applications we give extensions of a Sobolev restriction theorem.