Metal derivatives of azoles,part VII. Pyrazolato-bridged dinuclear complexes containing either cyclopalladated or -platinated trimesitylphosphine or -arsine

Summary The halogen bridges of the dimeric, cyclometallated trimesityl-arsine and -phosphine complexes of palladium(II) and platinum(II), where M=Pd or Pt and E=P or As have been replaced with pyrazolate groups to give the corresponding and less symmetric pyrazolato-bridged complexes, where M=Pd or Pt, E=P or As, Pz=pyrazolato anion, and M=Pd, E=As, Pz=3,5-dimethylpyrazolato anion. In the case of the palladium complexes,¹H. n.m.r. clearly indicates the presence of only one isomer which is most likely to have thetrans configuration while the platinum complexes are mixtures of bothcis andtrans forms.Part VI, ref. 3c     

Synthesis and characterization of poly-β-hydroxybutyrate. II. Synthesis of D-poly-β-hydroxybutyrate and the mechanism of ring-opening polymerization of β-butyrolactone

Synthesis of the naturally occurring polyester, D -poly-β-hydroxybutyrate (PHB) was accomplished by using an optically active monomer. Polymerization of D -(+)-β-butyrolactone (β-BL) of 73% optical purity with a catalyst system of Et₃Al–H₂O produced a polymer with a similar optical activity and essentially identical to the natural polymer as isolated from bacterial cells. This paper describes the synthesis and characterization of this optically active polyester along with a suggested mechanism to account for the observed stereospecific polymerization of β-BL with this catalyst system.     

Are dipolar liquids ferroelectric?

VH and HV depolarized hyper-Rayleigh scattering spectra were measured for liquid solutions of dipolar CH3CN in nondipolar C2Cl4 at T=300 K. The VH spectrum contains a strong narrow peak due to a slowly relaxing longitudinal orientation mode. This peak is absent in the HV spectrum, and it disappears from the VH spectrum when the CH3CN concentration is reduced to 8%. This observation is consistent with a ferroelectric phase transition predicted to occur when rho mu0(2)=9epsilon0kT=49 D2 M.     

p53 mutations in basal cell carcinomas arising in routine users of sunscreens

Sun exposure histories were obtained from a series of patients age 35 or younger following diagnosis and removal of a basal cell carcinoma (BCC). The DNA was extracted from tumor biopsy samples derived from BCC of 10 patients who reported that they did not use sunscreens during youth (age 18 or younger) and 10 patients who routinely employed sunscreens during this age period. Exons 5-9 of the p53 gene were then amplified in three fragments from these samples using a nested polymerase chain reaction (PCR) approach and screened for mutations using an RNA heteroduplex assay. All PCR products displaying evidence of a mutation were sequenced. It was found that 6 of the 10 patients who were not routine sunscreen users displayed mutations in these p53 exons. All of the mutations were located at dipyrimidine sites, five of the six were C-->T transitions and one mutation was a tandem double mutation, consistent with a role for solar UVB in BCC formation. In contrast, only one p53 mutation was detected in the group of 10 patients who routinely employed sunscreens during childhood and adolescence. Hence, a significantly (P = 0.029) lower level of p53 mutations was detected in the BCC obtained from sunscreen users compared with tumors derived from nonusers. These findings suggest that the mechanisms involved in the etiology of skin carcinogenesis differ in sunscreen users compared with people who did not routinely employ sunscreens. These data are also indicative of a protective effect associated with sunscreen use against the formation of p53 mutations. It is possible that the patients who were diagnosed with BCC despite their use of sunscreens possessed a genetic susceptibility for skin cancer formation and developed BCC through a p53-independent pathway. Alternatively, solar UVA wavelengths, that were generally not blocked by the suncare products employed by the sunscreen users, may have played a significant role in BCC development through induction of a mutation(s) in an oncogene and/or a tumor suppressor gene, other than p53, for these patients.     

Hyper-Rayleigh scattering spectrum of liquid nitromethane

The vertical vertical (VV), horizontal vertical (HV), and vertical horizontal (VH) hyper-Rayleigh scattering (HRS) spectra were measured for liquid CH3NO2 at T= 300 K. The main HRS spectral component has a width upsilon1=1.28 +/- 0.04 cm(-1), which gives an orientation relaxation time pi=4.1 +/- 0.1 ps in good agreement with other experiments. However, the VH spectrum also contains a previously unobserved strong narrow peak at zero-frequency shift, absent from the VV and HV spectra, which is due to a slowly relaxing longitudinal orientation mode. The upper bound on the width of this peak is 5 MHz, which corresponds to a relaxation time pi > 30 ns.     

Comparison of the major polypeptides of the erythrocyte nuclear envelope

The three most abundant nonhistone polypeptides (molecular weights 75,000, 71,000 and 61,000) of the avian erythrocyte nucleus have previously been isolated in the nuclear envelope fraction. They have been separated by sodium dodecylsulfate-polyacrylamide gel electrophoresis and peptide-mapped after limited enzymatic digestion. Three enzymes -- chymotrypsin, papain and Staphylococcus aureus protease -- were used. Results obtained with each enzyme indicate strong similarities between the three nuclear envelope polypeptides. The amino acid compositions of the two most abundant polypeptides (P75 and P71) have been determined and found to be similar. Further, they readily yield large fragments upon brief alkaline hydrolysis. For both P75, and P71 the degree and the pattern of alkaline fragmentation are almost identical. A 61,000-dalton polypeptide which appears to be P61 is obtained from P75 and P71 by mild acid hydrolysis. These results establish the close chemical similarity of these predominant polypeptides in the erythrocyte nucleus and suggest that they serve related functions.