249 research outputs found
Crystal structure determination as part of an ongoing undergraduate organic laboratory project: 5-[( E
Π ΠΠ€ΠΠ ΠΠΠ’ΠΠ«Π ΠΠΠΠ’ΠΠΠΠ§ΠΠ‘ΠΠΠ Π‘Π’Π Π£ΠΠ’Π£Π Π« ΠΠΠΠΠ«Π©ΠΠΠΠΠΠΠ Π―ΠΠΠ ΠΠΠΠ ΠΠΠΠΠ ΠΠΠ‘Π’Π ΠΠ Π ΠΠΠΠ‘Π’ΠΠΠ ΠΠΠ ΠΠΠΠΠ ΠΠ ΠΠ‘Π’ΠΠΠΠ ΠΠΠΠΠ Π‘ΠΠ―ΠΠΠ
Purpose: rationale for using bony landmarks of the femoral intercondylar space for an accurate determination of ACL attachment during arthroscopic reconstruction. Material and methods: anatomic research of 57 femur bones in which were studied anterior cruciate ligament femoral footprint, lateral intercondylar ridge and lateral bifurcate ridge. Results: research has shown, that lateral intercondylar ridge was present at 52 supervision (91 %), and its average length was 15.4 Β± 0.46 mm; lateral bifurcate ridge was determined in 28 (49 %), which average length was 3.95 Β± 0.26 mm. Conclusions: these bone formation can be considered as the reference structure for the identification of the anterior cruciate ligament femoral insertion.Π¦Π΅Π»Ρ ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΡ: ΠΎΠ±ΠΎΡΠ½ΠΎΠ²Π°Π½ΠΈΠ΅ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΡ Π°Π½Π°ΡΠΎΠΌΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΎΠ±ΡΠ°Π·ΠΎΠ²Π°Π½ΠΈΠΉ Π½Π°ΡΡΠΆΠ½ΠΎΠ³ΠΎ ΠΌΡΡΠ΅Π»ΠΊΠ° Π±Π΅Π΄ΡΠ΅Π½Π½ΠΎΠΉ ΠΊΠΎΡΡΠΈ Π² ΠΊΠ°ΡΠ΅ΡΡΠ²Π΅ Π²ΠΎΠ·ΠΌΠΎΠΆΠ½ΡΡ
ΠΎΡΠΈΠ΅Π½ΡΠΈΡΠΎΠ² Π΄Π»Ρ ΡΠΎΡΠ½ΠΎΠ³ΠΎ ΠΈΠ½ΡΡΠ°ΠΎΠΏΠ΅ΡΠ°ΡΠΈΠΎΠ½Π½ΠΎΠ³ΠΎ ΠΎΠΏΡΠ΅Π΄Π΅Π»Π΅Π½ΠΈΡ ΠΎΠ±Π»Π°ΡΡΠΈ ΠΏΡΠΈΠΊΡΠ΅ΠΏΠ»Π΅Π½ΠΈΡ ΠΠΠ‘. ΠΠ°ΡΠ΅ΡΠΈΠ°Π» ΠΈ ΠΌΠ΅ΡΠΎΠ΄Ρ: ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΎ 57 ΠΌΠ°ΡΠ΅ΡΠΈΡΠΎΠ²Π°Π½Π½ΡΡ
Π±Π΅Π΄ΡΠ΅Π½Π½ΡΡ
ΠΊΠΎΡΡΠ΅ΠΉ, Π½Π° ΠΊΠΎΡΠΎΡΡΡ
Π°Π½Π°ΡΠΎΠΌΠΈΡΠ΅ΡΠΊΠΈΠΌ ΠΌΠ΅ΡΠΎΠ΄ΠΎΠΌ ΠΈΠ·ΡΡΠ΅Π½Ρ ΠΎΡΠΎΠ±Π΅Π½Π½ΠΎΡΡΠΈ ΠΎΠ±Π»Π°ΡΡΠΈ ΠΏΡΠΈΠΊΡΠ΅ΠΏΠ»Π΅Π½ΠΈΡ ΠΏΠ΅ΡΠ΅Π΄Π½Π΅ΠΉ ΠΊΡΠ΅ΡΡΠΎΠΎΠ±ΡΠ°Π·Π½ΠΎΠΉ ΡΠ²ΡΠ·ΠΊΠΈ, Π»Π°ΡΠ΅ΡΠ°Π»ΡΠ½ΡΠΉ ΠΌΠ΅ΠΆΠΌΡΡΠ΅Π»ΠΊΠΎΠ²ΡΠΉ ΠΊΡΠ°ΠΉ ΠΈ Π»Π°ΡΠ΅ΡΠ°Π»ΡΠ½ΡΠΉ Π±ΠΈΡΡΡΠΊΠ°ΡΠΈΠΎΠ½Π½ΡΠΉ ΠΊΡΠ°ΠΉ. Π Π΅Π·ΡΠ»ΡΡΠ°ΡΡ: Π»Π°ΡΠ΅ΡΠ°Π»ΡΠ½ΡΠΉ ΠΌΠ΅ΠΆΠΌΡΡΠ΅Π»ΠΊΠΎΠ²ΡΠΉ ΠΊΡΠ°ΠΉ ΠΏΡΠΎΡΡΠΆΠ΅Π½Π½ΠΎΡΡΡΡ 15.4 Β± 0.46 ΠΌΠΌ ΠΎΠ±Π½Π°ΡΡΠΆΠ΅Π½ Π½Π° 52 ΠΏΡΠ΅ΠΏΠ°ΡΠ°ΡΠ°Ρ
(91%), Π»Π°ΡΠ΅ΡΠ°Π»ΡΠ½ΡΠΉ Π±ΠΈΡΡΡΠΊΠ°ΡΠΈΠΎΠ½Π½ΡΠΉ ΠΊΡΠ°ΠΉ Π΄Π»ΠΈΠ½ΠΎΠΉ 3.95 Β± 0.26 ΠΌΠΌ ΠΎΡΠΌΠ΅ΡΠ΅Π½ Π½Π° 28 ΠΊΠΎΡΡΡΡ
(49%). ΠΡΠ²ΠΎΠ΄Ρ: Π΄Π°Π½Π½ΡΠ΅ ΠΊΠΎΡΡΠ½ΡΠ΅ ΠΎΠ±ΡΠ°Π·ΠΎΠ²Π°Π½ΠΈΡ ΠΌΠΎΠ³ΡΡ ΡΠ°ΡΡΠΌΠ°ΡΡΠΈΠ²Π°ΡΡΡΡ ΠΊΠ°ΠΊ ΡΠ΅ΡΠ΅ΡΠ΅Π½ΡΠ½ΡΠ΅ ΡΡΡΡΠΊΡΡΡΡ Π΄Π»Ρ ΠΈΠ΄Π΅Π½ΡΠΈΡΠΈΠΊΠ°ΡΠΈΠΈ ΠΌΠ΅ΡΡΠ° ΠΏΡΠΈΠΊΡΠ΅ΠΏΠ»Π΅Π½ΠΈΡ ΠΠΠ‘ ΠΊ Π±Π΅Π΄ΡΠ΅Π½Π½ΠΎΠΉ ΠΊΠΎΡΡΠΈ
CORRELATION OF THE SKULL PARAMETERS WITH THE WIDTH OF THE DENTAL ARCHES
The study of regularities and variant anatomy in the structure of organs and parts of the human body is one of the fundamental problems of morphology having an applied orientation. The main method of studying a person's aesthetics is a morphometric examination of the head. It includes the study of its size, size and shape of the face and its individual parts, as well as the relationship between the size and shape of the skull and dental arches. The main linear parameters of the skull and their interrelations with the parameters of the width of the dental arches of the upper jaw are studied on the skull of male of mature age with physiological occlusion of teeth. The study was carried out taking into account the type of skull. It was revealed that the index of the width of the dental arch from the vestibular side is lesser then the index of the upper face and the intergnatic part in the frontal part, and in the distal part - to the contrary. Indicators of the width of the dental arch from the palatal side were less in their values to the parameters of the skull at all levels of measurement in all craniotypes. Obtained data on the width of the dental arch of the upper jaw, linear parameters of the skull and their interrelations expand and deepen the information available in the literature on the dimensional characteristics of the craniofacial complex
The structure and characteristics of photochromic dithienylethenes
Abstract. The data on X-ray diffraction analysis for dihetarylethenes with perfluorocyclopentene (F), maleic anhydride (M) and cyclobutenedione (S) bridges between thienyl fragments were summarized and their photochromic properties were discussed. It was established that benzoxazole and benzothiazole substituents in position 5 of thienyl rings are coplanar to the plane of thiophene cycles. Thienyl fragments in A form of all dithienylethenes are considerably turned relative to the plane of bridging cycle. It means that there is no conjugation between Ο -electrons of aromatic heterocycles and double bond of the bridge. Flattening of molecule framework and the envelope conformation of thienyl cycles because of aromaticity loss are characteristic features of the form B structure with F-bridge. In all cases (excluding the compounds with alkylthio substituents in position 2 of thiophene cycle) the photochromic transition A ββ B is observed independently of different nature and structure of functional groups
Photochromic properties of composite films of thermally irreversible diarylethenes and fulgimides in polytetrafluoroethylene matrix
Photochromic polymeric thin films have been prepared by vacuum codeposition
of polytetrafluoroethylene (PTFE) and thermally irreversible photochromic
compounds: the cyclopentene derivative of diarylethene and fulgimide. Their
photochromic properties were studied using the spectral-kinetic method as compared
with polymethyl methacrylate (PMMA) films filled with the same photochromic
compounds prepared using the spin coating method. The films prepared using codeposition
in vacuum are characterized by photochromic properties acceptable for
recording media for 3D optical memor
Modern views of facial asymmetry
The peculiarities of functional asymmetry of the face 46 men aged 20-22 years. Set neravnoznachnost the left and right parts of the face, one of which is taller and wider and the other narrower and lower. Mimic asymmetry is caused by differences of innervation and it appears through particularities of mimics, while functional asymmetry depends on the asymmetry of the brain and is characterized by a more active expressiveness of facial muscles.ΠΠ·ΡΡΠ΅Π½Ρ ΠΎΡΠΎΠ±Π΅Π½Π½ΠΎΡΡΠΈ ΡΡΠ½ΠΊΡΠΈΠΎΠ½Π°Π»ΡΠ½ΠΎΠΉ Π°ΡΠΈΠΌΠΌΠ΅ΡΡΠΈΠΈ Π»ΠΈΡΠ° 46 ΠΌΡΠΆΡΠΈΠ½ Π² Π²ΠΎΠ·ΡΠ°ΡΡΠ΅ 20-22 Π»Π΅Ρ. Π£ΡΡΠ°Π½ΠΎΠ²Π»Π΅Π½Ρ Π½Π΅ΡΠ°Π²Π½ΠΎΠ·Π½Π°ΡΠ½ΠΎΡΡΡ ΠΏΡΠ°Π²ΠΎΠΉ ΠΈ Π»Π΅Π²ΠΎΠΉ ΡΠ°ΡΡΠ΅ΠΉ Π»ΠΈΡΠ°, ΠΎΠ΄Π½Π° ΠΈΠ· ΠΊΠΎΡΠΎΡΡΡ
ΡΠΈΡΠ΅ ΠΈ Π²ΡΡΠ΅, Π΄ΡΡΠ³Π°Ρ - ΡΠΆΠ΅ ΠΈ Π½ΠΈΠΆΠ΅. ΠΠΈΠΌΠΈΡΠ΅ΡΠΊΠ°Ρ Π°ΡΠΈΠΌΠΌΠ΅ΡΡΠΈΡ ΡΠ²ΡΠ·Π°Π½Π° Ρ ΡΠ°Π·Π»ΠΈΡΠΈΠ΅ΠΌ ΠΈΠ½Π½Π΅ΡΠ²Π°ΡΠΈΠΈ ΠΈ ΠΏΡΠΎΡΠ²Π»ΡΠ΅ΡΡΡ ΠΎΡΠΎΠ±Π΅Π½Π½ΠΎΡΡΡΠΌΠΈ ΠΌΠΈΠΌΠΈΠΊΠΈ, Π² ΡΠΎ Π²ΡΠ΅ΠΌΡ ΠΊΠ°ΠΊ ΡΡΠ½ΠΊΡΠΈΠΎΠ½Π°Π»ΡΠ½Π°Ρ Π°ΡΠΈΠΌΠΌΠ΅ΡΡΠΈΡ Π·Π°Π²ΠΈΡΠΈΡ ΠΎΡ Π°ΡΠΈΠΌΠΌΠ΅ΡΡΠΈΠΈ ΠΌΠΎΠ·Π³Π° ΠΈ Ρ
Π°ΡΠ°ΠΊΡΠ΅ΡΠΈΠ·ΡΠ΅ΡΡΡ Π±ΠΎΠ»Π΅Π΅ Π°ΠΊΡΠΈΠ²Π½ΠΎΠΉ Π²ΡΡΠ°Π·ΠΈΡΠ΅Π»ΡΠ½ΠΎΡΡΡΡ ΠΌΠΈΠΌΠΈΡΠ΅ΡΠΊΠΎΠΉ ΠΌΡΡΠΊΡΠ»Π°ΡΡΡΡ
Heteroleptic Ir(III) complexes based on 2-(2,4-difluorophenyl)-pyridine and bisthienylethene: structures, luminescence and photochromic properties
Two bisthienylethenes 2-(2-hydroxyphenyl)-4,5-bis[2,5-dimethyl(3-thienyl)]-1H-imidazole (L1H) and 2-(2-hydroxyphenyl)-4,5-bis(2,5-dimethyl(3-thienyl))-1-phenyl-imidazole (L2H), which have a chelating N,O-donor binding site attached to the photochromic core, have been synthesized using a one-pot condensation reaction, and used to prepare the heteroleptic complexes [Ir(dfppy)2(L1)]Β·2CH3OH (1) and [Ir(dfppy)2(L2)] (2) [dfppyH = 2-(2,4-difluorophenyl)-pyridine]. In the crystal structures of all four compounds, two thiophene groups of each bisthienylethene molecule adopt parallel conformation. Neighboring molecules in L1H and 1 are linked into supramolecular chains through hydrogen bonds. Particularly, the packing structure of 1 contains right- and left-handed 21 helical chains. In contrast, neighboring molecules in L2H and 2 interact only through van der Waals interactions. At room temperature, L1H and L2H in CH2Cl2 show fluorescence emission at 442 nm and 469 nm, respectively. Compounds 1 and 2 in CH2Cl2 reveal broad emission band characteristics of the Ir(III)/dfppyβ chromophores at 508 nm and 494 nm, respectively, with a mixing of 3MLCT and 3LC characters. At room temperature, the photochromism ability of L2H in CH2Cl2 is clearly weaker than that of L1H. Moreover, no photochromism has been observed in 1 and 2. It has been demonstrated that both the substituent group and {Ir(dfppy)2}+ coordination could significantly influence the crystal structures, luminescence and photochromic properties of L1H, L2H, 1 and 2
Thermally irreversible photochromic dithienylethenes
Abstract. A lot of previously unknown derivatives of dithienylperfluorocyclopentene (DTPFCP) were synthesized. It was shown that 2, 2 -dialkylsubstituted DTPFCP'S are phtochromes. The quantum yields of forward and backward photochemical reactions and spectral parameters of open and cyclic forms of the photochromes synthesized were measured. An attempt to obtain fluorescing phtochromes by means of introduction of benzoxazolyl, benzthiazolyl and 1,2,4-oxadiazolyl moieties in 5 and 5 positions of DTPFCP failed; these compounds were synthesized but they do not fluoresce
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