The present invention relates to chemical compositions comprising imidazolinone compounds that are suitable for use in turfgrass management. The invention also provides methods for altering the growth and reducing mowing frequency, suppressing seed head formation and controlling undesirable vegetation in turfgrass.
|
3. A method for retarding growth and suppressing seed heading in a turfgrass, the method comprising: applying to the foliage or soil surrounding the turfgrass, a sufficient quantity of a composition having an mount of 2-(4'-isopropyl-4-methyl-5-oxo -2-imidazolin-2-yl)-5-methyl-nicotinic acid or salt thereof.
5. A method for retarding growth and suppressing seedheading in turfgrasses, which comprises applying to the foliage or soft surrounding the turfgrasses, a sufficient quantity of a composition having a synergistic effective amount of at least one compound comprising the structure: ##STR10## wherein X is N or CH; r is H, C1 #6# -C4 alkyl, or a cation; r1 and r2 are each H, C1 -C4 alkyl, C1 -C4 alkyloxy, C3 -C6 alkenyloxy, or r1 and r2 taken together with the carbons to which they are attached may form a 6 membered ring; and the optical isomer thereof.
1. A method for retarding growth and suppressing seed heading in turfgrasses, which comprises applying to the foliage or soil surrounding said turfgrasses a composition comprising a solid or liquid diluent and an imidazolinone compound, in an mount sufficient to retard growth and suppress seedheading in turfgrass, having the structure: ##STR7## wherein X is N or CR3 #6# ; r is hydrogen; C1 -C12 alkyl optionally substituted with one of the following groups: C1 -C4 alkoxy, halogen, hydroxyl, C3 -C6 cycloalkyl, benzyloxy, furyl, phenyl, halophenyl, C1 -C4 alkylphenyl, C1 -C4 alkoxyphenyl, nitrophenyl, carboxyl, C1 -C3 alkoxycarbonyl, cyano or tri(C1 -C3) alkylammonium;
C3 -C12 alkenyl optionally substituted with one of the following groups: C1 -C3 alkoxyl, phenyl, halogen or C1 -C3 alkoxycarbonyl, or with two C1 -C4 alkoxy groups or two halogen atoms; C3 -C6 cycloalkyl optionally substituted with one or two C1 -C3 alkyl groups; C3 -C10 alkynyl; or a cation; r1 and r2 are each hydrogen, halogen, C1 -C6 alkyl, C1 -C4 hydroxyalkyl, C1 -C6 alkoxy, C1 -C4 alkythio, phenoxy, C1 -C4 haloalkyl, OCF2 CHF2, OCF3, OCHF2, nitro, cyano, C1 -C4 alkylsulfonyl, NR4 r5, C3 -C8 straight or branched alkenyloxy optionally substituted with one to three halogens, C3 -C8 straight or branched alkynyloxy optionally substituted with one to three halogens, or phenyl optionally substituted with one C1 -C4 alkyl, C1 -C4 alkoxy or halogen; r3 is hydrogen, halogen, C1 -C4 alkyl, C1 -C4 alkythio, C1 -C4 alkoxyl, CF3, NO2, OCF3, OCHF2 or OCF2 CHF2 ; r4 is hydrogen or C1 -C4 alkyl; r5 is C1 -C4 alkyl; and, when taken together, r1 and r2, in the case of X═CR3, may form a ring in which r1 r2 is represented by (1) the structure: --(CH2)n --, where n is an integer of 2, 3 or 4; or (2) by the structure: ##STR8## where L, M, r6 and r7 each represent hydrogen; halogen, C1 -C4 alkyl or C1 -C3 alkoxy; and, in the case of X═N, r1 r2 (1) may form a ting in which r1 r2 is represented by the structure --(CH2)n --, where n is an integer of 3 or 4; or (2) when taken together with the carbons to which they are attached may form a 5-membered ring containing one O or S; or (3) may form a ring represented by the structure; ##STR9## where L, M, r6 and r7 each represent hydrogen, halogen, C1 -C4 alkyl, C1-C4 alkoxy, C1 -C4 alkylthio, C1 -C4 alkylsulfonyl, C1 -C4 haloalkyl, NO2, CN, phenyl, phenoxy, amino, C1 -C4 alkylamino, diloweralkylamino, chlorophenyl, methylphenyl, phenoxy substituted with one Cl, CF3, NO2 or CH3 group, OCF2 CHF2, OCF3, OCHF2, C3 -C8 straight or branched alkenyloxy optionally substituted with one to three halogens, or C3 -C8 straight or branched alkynyloxy optionally substituted with one to three halogens; or an N-oxide thereof when X═N provided that r cannot be alkenyl or alkynyl and r1 and r2 cannot be NR4 r5 or alkylthio; an optical isomer thereof or a mixture of region isomers thereof, alone and in combination with N-[2,4-dimethyl-5[[(trifluoromethyl) sulfonyl]amino]phenyl]-acetamide.
2. The method of
4. The method of
6. The method of
7. The method of
8. The method of
9. The method of
10. The method of
11. The method of
|
|||||||||||||||||||||||||||||
This application is a division of Ser. No. 235,937, filed May 2, 1994, U.S. Pat. No. 5,591,693, which is a division of Ser. No. 833,221, filed Feb. 10, 1992, U.S. Pat. No. 5,340,791, which is a division of Ser. No. 411,444, filed Sep. 22, 1989, U.S. Pat. No. 5,116,403, which is a continuation of Ser. No. 818,591, filed Jan. 15, 1986, abandoned, which is a continuation-in-part of Ser. No. 698,191, filed Feb. 4, 1985, abandoned,
Maintenance of lawns, sport fields, playgrounds, parks, golf courses, roadsides and cemeteries represents a growing area of interest. The annual investment in time, labor, chemical treatments, fertilization and equipment for the maintenance of turfgrasses was shown in 1965 to be over 4.2 billion dollars. Additionally, it was shown in 1965 that about 50% of total annual lawn care expenditures was almost equally divided between labor (23.5%) and equipment (26.5%).
Since a significant portion of the investment in turfgrass management is devoted to labor costs, and the cost associated with purchasing, maintaining and operating maintenance equipment, it would be highly desirable to be able to supplement turfgrass management practices with chemical treatments which reduce the maintenance requirements of the grass. The development and use of chemical treatments which retard the growth of grass, and hence the frequency of mowing, reduce and inhibit heading, control undesirable weeds and are not injurious to the grass and do not alter its appearance could significantly reduce the overall maintenance costs for turfgrass management.
Advances in the development of chemical herbicide treatments for the control of weeds have resulted in a wide variety of chemicals which are suitable for weed control in turf. Advances in the field of plant growth regulators have resulted in the discovery that certain of these chemicals are suitable for use on turfgrasses. For example, mefluidide, (Embark®)N-[2,4-dimethyl-5-[[(trifluoromethyl)sulfonyl]amino]phenyl]ac etamide, a plant growth regulator produced by 3M Company, is registered for use as a growth and development retardant on turf and ornamental species. More recently, work in the area of turfgrass treatment has resulted in the evaluation of mixtures of chemicals in an attempt to enhance effects, improve safety margins, obtain several effects at the same time, reduce rates of application or alter the effect obtained on one specific species.
Certain chemical combinations useful as turfgrass treatments were reported by K. J. Tautvydas in the Proceedings of Tenth Annual Meeting of the Plant Growth Regulator Society, 1983. This article discloses synergistic growth retardation of Kentucky bluegrass and johnsongrass with certain mixtures of mefluidide and chlorsulfuron, 2-chloro-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]benzenesu lfonamide, and a similar effect on bluegrass, johnsongrass and bermudagrass with certain mixtures of mefluidide and methyl 2-[[[[(4,6-dimethyl-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]benzoate.
While it is clear that a great deal of research and progress is being made in developing chemical compositions to aid in total turf management programs, it is also becoming clear that, due to variations in climatic conditions and differences in preferred grass varieties within these different growing regions, different treatments will probably be required on a region-to-region and species-to-species basis.
It is an object of this invention to provide chemical compositions containing certain imidazolinone compounds of the formula (I) ##STR1## wherein X is N or CR3 ; R is hydrogen; C1 -C12 alkyl optionally substituted with one of the following groups: C1 -C4 alkoxy, halogen, hydroxy, C3 -C6 cycloalkyl, benzyloxy, furyl, phenyl, halophenyl, C1 -C4 alkylphenyl, C1 -C4 alkoxyphenyl, nitrophenyl, carboxyl, C1 -C3 alkoxycarbonyl, cyano, or tri(C1 -C3)alkylammonium;
C3 -C12 alkenyl optionally substituted with one of the following groups: C1 -C3 alkoxy, phenyl, halogen, or C1 -C3 alkoxycarbonyl or with two C1 -C4 alkoxy groups or two halogen atoms;
C3 -C6 cycloalkyl optionally substituted with one or two C1 -C3 alkyl groups;
C3 -C10 alkynyl; or
a cation;
R1 and R2 are each hydrogen, halogen, C1 -C6 alkyl, C1 -C4 hydroxyalkyl, C1 -C6 alkoxy, C1 -C4 alkylthio, phenoxy, C1 -C4 haloalkyl, OCF2 CHF2, OCF3, OCHF2, nitro, cyano, C1 -C4 alkylsulfonyl, NR4 R5, C3 -C8 straight or branched alkenyloxy optionally substituted with one to three halogens, C3 -C8 straight or branched alkynyloxy optionally substituted with one to three halogens, or phenyl optionally substituted with one C1 -C4 alkyl, C1 -C4 alkoxy or halogen;
R3 is hydrogen, halogen, C1 -C4 alkyl, C1 -C4 alkylthio, C1 -C4 alkoxy, CF3, NO2, OCF3, OCHF2, or OCF2 CHF2 ;
R4 is hydrogen or C1 -C4 alkyl;
R5 is C1 -C4 alkyl;
and, when taken together, R1 and R2, in the case of X═CR3, may form a ring in which R1 R2 is represented by
(1) the structure: --(CH2)n --, where n is an integer of 2, 3 or 4; or
(2) by the structure: ##STR2## where L, M, R6 and R7 each represent hydrogen, halogen, C1 -C4 alkyl or C1 -C3 alkoxy;
and, in the case of X═N, R1 and R2
(1) may form a ring in which R1 R2 is represented by the structure --(CH2)n --, where n is an integer of 3' or 4; or
(2) when taken together with the carbons to which they are attached may form a 5-membered ring containing one O or S; or
(3) may form a ring represented by the structure: ##STR3## where L, M, R6 and R7 each represent hydrogen, halogen, C1 -C4 alkyl, C1 -C4 alkoxy, C1 -C4 alkylthio, C1 -C4 alkylsulfonyl, C1 -C4 haloalkyl, NO2, CN, phenyl, phenoxy, amino, C1 -C4 alkylamino, diloweralkylamino, chlorophenyl, methylphenyl, phenoxy substituted with one Cl, CF3, NO2, or CH3 group, OCF2 CHF2, OCF3, OCHF2, C3 -C8 straight or branched alkenyloxy optionally substituted with one to three halogens, or C3 -C8 straight or branched alkynyloxy optionally substituted with one to three halogens; and the N-oxides thereof when X═N, provided that R cannot be alkenyl or alkynyl and R1 and R2 cannot be NR4 R5 or alkylthio, and the optical isomers thereof and mixtures of region isomers thereof,
alone and in combination with 2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)nicotinic acid or salts thereof, maleic hydrazide, N-[2,4-dimethyl-5-[[(trifluoromethyl)sulfonyl]amino]phenyl]acetamide, 2-chloro-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]benzenesu lfonamide or methyl 2-[[[[(4,6-dimethyl-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]benzoate and mixtures thereof, which provide compositions that reduce growth in a variety of grass species, without being injurious, inhibit seed heading, and control certain weeds, and further that the desired effect or group of effects for a given variety of grass under specific growing conditions may be obtained by altering the combination and rate of each component.
The imidazolinone compounds suitable for use in turf described in U.S. Pat. No. 4,188,487, pending applications for U.S. Letters patent Ser. Nos. 382,041, 616,747, 631,283, 611,191 and pending application for U.S. Letters patent, Ser. No. 635,787 as herbicides and plant growth regulators for increasing crop yields. Surprisingly, it has been found that compounds represented by Formula (I) are efficacious for retarding the growth of turf and suppressing seed heads. Additionally, it has been found that the longevity of the effect and the extent of the effect may be increased significantly by applying formula (I) compounds in combination with one or more of 2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)nicotinic acid or salts thereof, maleic hydrazide, N-[2,4-dimethyl-5-[[(trifluoromethyl)sulfonyl]amino]-phenyl]acetamide, 2-chloro-N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl )aminocarbonyl]benzenesulfonamide and methyl 2-[[[[(4,6-dimethyl-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]benzoate. Further, it has been found that by altering the rates of each of the components, the desirable effects of growth retardation, head inhibition and control of certain weeds may be obtained in a variety of grass species without being injurious to the grass. Preferred compounds suitable for use in turfgrass management compositions of the invention are illustrated in Table I below.
| TABLE I |
| ______________________________________ |
| Component |
| ______________________________________ |
| ##STR4## |
| (a) X R R1 R2 |
| N H H OCH3 |
| (b) N H CHCHCHCH |
| CH CH3 |
| CH3 H |
| (c) + |
| CH CH3 |
| H CH3 |
| (d) N H OCH2 CHCH2 |
| H |
| (e) N H CH2CH2O |
| (f) N C2 H5 |
| OCH3 H |
| (g) N H |
| ##STR5## |
| (h) N H C2 H5 |
| H |
| (i) N H |
| phenyl H |
| (j) N H |
| ##STR6## |
| (k) N CH3 |
| H OCH3 |
| 2 2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin- |
| 2-yl)nicotinic acid |
| 3 maleic hydrazide |
| 4 N-['2,4-dimethyl-5-[[(trifluoromethyl)- |
| sulfonyl]amino]phenyl]acetamide |
| 5 chlorsulfuron, 2-chloro-N-[(4-methoxy-6- |
| methyl-1,3,5-triazin-2-yl)aminocarbonyl]- |
| benzenesulfonamide |
| 6 methyl 2-[[[[(4,6-dimethyl-2-pyrimidinyl)- |
| amino]carbonyl]amino]sulfonyl]benzoate |
| ______________________________________ |
As indicated above, the composition of the invention may be altered to obtain different effects or the same set of effects on a different grass species without injuring the grass. The preferred ranges of rates for each of the components are illustrated in Table II below,
| TABLE II |
| ______________________________________ |
| Preferred rate ranges for turf management |
| compositions of the invention |
| Composition Rate grams/hectare |
| ______________________________________ |
| 1 5 to 500 |
| 2 0.1 to 200 |
| 1 + 2 5 to 250 + 0.25 to 2 |
| 1 + 3 5 to 250 + 20 to 5000 |
| 1 + 4 5 to 250 + 20 to 500 |
| 1 + 5 5 to 250 + 0.25 to 20 |
| 1 + 6 5 to 250 + 0.25 to 20 |
| 1 + 2 + 4 1 to 250 + 0.25 to 25 + 20 to 500 |
| 1 + 2 + 5 1 to 250 + 0.25 to 25 + 0.25 to 20 |
| 1 + 2 + 6 1 to 250 + 0.25 to 25 + 0.25 to 20 |
| ______________________________________ |
As discussed above, by adjusting the rates of each component the compositions may be used on a variety of species as indicated in Table III below.
| TABLE III |
| __________________________________________________________________________ |
| Adjusting Composition for different grass species. |
| Composition |
| Bermudagrass |
| Bluegrass |
| Fescue Rye |
| __________________________________________________________________________ |
| 1 5.0 to 500.0* |
| 5.0 to 500.0 |
| 5.0 to 250.0 |
| 5.0 to 250.0 |
| 2 5.0 to 200.0 |
| 0.1 to 20.0 |
| 0.1 to 10.0 |
| 0.1 to 10.0 |
| 1 + 2 5.0 to 250.0 + |
| 5.0 to 250.0 + |
| 5.0 to 150.0 + |
| 5.0 to 150.0 + |
| 0.25 to 25.0 |
| 0.25 to 25.0 |
| 0.5 to 10.0 |
| 0.5 to 10.0 |
| 1 + 3 5.0 to 250.0 + |
| 5.0 to 250.0 + |
| 5.0 to 150.0 + |
| 5.0 to 150.0 to |
| 20.0 to 5000.0 |
| 20.0 to 5000.0 |
| 20.0 to 2500.0 |
| 20.0 to 2500.0 |
| 1 + 4 50.0 to 250.0 + |
| 5.0 to 250.0 + |
| 5.0 to 150.0 + |
| 5.0 to 150.0 + |
| 0.25 to 10.0* |
| 6.25 to 10.0 |
| 0.25 to 5.0 |
| 0.25 to 5.0 |
| 1 + 5 5.0 to 250.0 + |
| 5.0 to 250.0 + |
| 5.0 to 150.0 + |
| 5.0 to 150.0 + |
| 0.25 to 10.0 * |
| 0.25 to 10.0 |
| 0.25 to 5.0 |
| 0.25 to 5.0 |
| 1 + 6 5.0 to 250.0 + |
| 5.0 to 250.0 + |
| 5.0 to 150.0 + |
| 5.0 to 150.0 + |
| 0.25 to 10.0 |
| 0.25 to 10.0 |
| 0.25 to 5.0 |
| 0.25 to 5.0 |
| 1 + 2 + 4 |
| 1 to 250 + |
| 1 to 250 + |
| 1 to 250 + |
| 1 to 250 + |
| 0.25 to 25 + |
| 0.25 to 25 + |
| 0.25 to 10 + |
| 0.25 to 10 + |
| 20 to 500 |
| 20 to 500 |
| 20 to 500 |
| 20 to 250 |
| 1 + 2 + 5 |
| 1 to 250 + |
| 1 to 250 + |
| 1 to 250 + |
| 1 to 250 + |
| 0.25 to 25 + |
| 0.25 to 25 + |
| 025 to 25 + |
| 0.25 to 25 + |
| 0.25 to 10 |
| 0.25 to 10 |
| 0.25 to 5 |
| 0.25 to 5 |
| 1 + 2 + 6 |
| 1 to 250 + |
| 1 to 250 + |
| 1 to 250 + |
| 1 to 250 + |
| 0.25 to 25 + |
| 0.25 to 25 + |
| 0.25 to 25 + |
| 0.25 to 25 + |
| 0.25 to 10 |
| 0.25 to 10 |
| 25 + 0.25 to 5 |
| 0.25 to 5 |
| __________________________________________________________________________ |
| *Rate in grams/hectare |
The compositions of the invention may conveniently be applied by post-emergence treatment of the grass. They may be applied as a mixture of all the ingredients or as sequential treatments. Since the formula (I) compounds wherein R is hydrogen are acids, as is 2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)nicotinic acid and these compounds may be applied as salts of the acid wherein R is a salt-forming cation, the compositions may be applied as aqueous solutions and suspensions containing non-ionic surfactants, and wetting agents which may be prepared by introducing the components directly to water or by adding formulations such as concentrates, suspensions, emulsions, wettable powders, dispersible granules and the like to water prior to application. Additionally granular compositions containing some of the compositions of the invention may be applied to the turf followed by additional post-emergence treatments as required. The invention is further illustrated by the following non-limiting examples.
PAC Evaluation of Compositions of the Invention for Retarding GrowthSeeds of the grass variety to be evaluated are tumbled for three minutes with soil at a rate of 7 ounces of seed per 100 lbs of greenhouse soil comprising a mixture by weight of sand (32%), silt (48%), and clay (20%). A layer of this seed mixture one-half inch thick is placed in a four inch diameter pot containing greenhouse soil and the plants are allowed to germinate and grow for six to eight weeks prior to treatment. The plants are clipped to a height of one-half inch and are sprayed with 100 mL of an aqueous solution containing 0.25% by volume of a nonionic surfactant mixture alkylarylpolyoxyethyleneglycols, free fatty acids and 2-propanol, and the formula I (a)-(k) compounds and compounds 2, 3, 4, and 5 both alone and in combinations at various spray rates. Each treatment is applied to three pots and the pot randomly placed in a greenhouse where the plants are cared for employing standard greenhouse procedures. Three weeks after treatment the plants are clipped to a height of one-half inch and the clippings are dried in an oven for 48 hours at 90°C and the dry weight of clippings for each treatment is recorded. Examination of Tables IV and V below which is a summary of results obtained on tall fescue and bermudagrass, respectively, clearly demonstrates the effectiveness of the formula I (a)-(k) compounds alone and additionally demonstrates the improved effectiveness of these formula I (a)-(k) compounds in combination with compounds 2, 3, 4 and 5 for retarding the growth of turfgrasses as measured by dry clipping weight.
| TABLE IV |
| ______________________________________ |
| Greenhouse evaluation of compositions of |
| the invention on tall fescue (Festuca arundinaceae) |
| Rate(s) % Decrease in |
| Treatments g or lb/A dry wt of clipping |
| ______________________________________ |
| 1(h) 20.0 g 37 |
| 1(h) 40.0 g 51 |
| 2 1.0 g 2 |
| 2 2.0 g 3 |
| 1(j) 20.0 g 29 |
| 1(j) 40.0 g 32 |
| 1(j) 60.0 g 25 |
| 1(h) + 2 20.0 g + 1.0 g |
| 52 |
| 1(h) + 2 20.0 g + 2.0 g |
| 52 |
| 1(h) + 2 40.0 g + 1.0 g |
| 37 |
| 1(h) + 2 40.0 g + 2.0 g |
| 76 |
| 4 0.125 lb 6 |
| 4 0.375 lb 59 |
| 1(h) + 4 20.0 g + 0.125 lb |
| 80 |
| 1(j) + 4 40.0 g + 0.125 lb |
| 82 |
| 1(j) + 4 20.0 g + 0.125 lb |
| 60 |
| 1(j) + 4 40.0 g + 0.125 lb |
| 46 |
| 1(j) + 4 60.0 g + 0.125 lb |
| 64 |
| 3 1.5 lb 2 |
| 3 3.0 lb 7 |
| 1(h) + 3 20.0 g + 1.5 lb |
| 45 |
| 1(h) + 3 40.0 g + 1.5 lb |
| 66 |
| 1(j) + 3 20.0 g + 1.5 lb |
| 70 |
| 1(j) + 3 20.0 g + 1.5 lb |
| 70 |
| 1(j) + 3 40.0 g + 1.5 lb |
| 49 |
| 1(j) + 3 60.0 g + 1.5 lb |
| 46 |
| ______________________________________ |
| TABLE V |
| ______________________________________ |
| Greenhouse evaluation of compositions of the invention |
| on burmudagrass (Cynodon sp) |
| Rates % Decrease in |
| Treatments (grams/Acre) |
| dry wt of clippings |
| ______________________________________ |
| 1(h) 5.0 15.3 |
| 1(h) 10.0 14.7 |
| 1(h) 15.0 12.7 |
| 1(h) 20.0 12.7 |
| 1(h) 40.0 57.3 |
| 1(h) 100.0 71.3 |
| 2 2.00 24.7 Increase |
| 2 4.00 8.0 Increase |
| 2 6.00 59.3 |
| 2 8.00 82.0 |
| 1(h) + 2 5.0 + 2.0 19.3 |
| 1(h) + 2 5.0 + 4.0 44.7 |
| 1(h) + 2 5.0 + 8.0 82.0 |
| 1(h) + 2 10.0 + 0.5 |
| 34.0 |
| 1(h) + 2 10.0 + 1.0 |
| 5.3 |
| 1(h) + 2 10.0 + 2.0 |
| 38.7 |
| 1(h) + 2 10.0 + 4.0 |
| 52.0 |
| 1(h) + 2 10.0 + 6.0 |
| 86.0 |
| 1(h) + 2 10.0 + 8.0 |
| 86.7 |
| 1(h) + 2 15.0 + 0.25 |
| 38.7 |
| 1(h) + 2 15.0 + 0.5 |
| 18.7 |
| 1(h) + 2 15.0 + 1.0 |
| 2.0 Increase |
| 1(h) + 2 15.0 + 2.0 |
| 8.0 Increase |
| 1(h) + 2 15.0 + 4.0 |
| 10.7 |
| 1(h) + 2 15.0 + 6.0 |
| 83.3 |
| 1(h) + 2 15.0 + 8.0 |
| 78.0 |
| 1(h) + 2 20.0 + 0.25 |
| 48.7 |
| 1(h) + 2 20.0 + 0.5 |
| 16.7 |
| 1(h) + 2 20.0 + 1.0 |
| 18.0 |
| 1(h) + 2 20.0 + 2.0 |
| 54.0 |
| 1(h) + 2 20.0 + 4.0 |
| 45.3 |
| 1(h) + 2 20.0 + 6.0 |
| 66.7 |
| 1(h) + 2 25.0 + 0.25 |
| 7.3 |
| 1(h) + 2 25.0 + 0.50 |
| 27.3 |
| 1(h) + 2 25.0 + 1.0 |
| 36.7 |
| 1(h) + 2 25.0 + 2.0 |
| 75.3 |
| 1(h) + 2 25.0 + 4.0 |
| 76.0 |
| 1(h) + 2 30.0 + 6.0 |
| 88.0 |
| 1(h) + 2 30.0 + 0.25 |
| 36.7 |
| 1(h) + 2 30.0 + 0.50 |
| 20.0 |
| 1(h) + 2 30.0 + 1.0 |
| 42.7 |
| 1(h) + 2 30.0 + 2.0 |
| 78.0 |
| 1(h) + 2 30.0 + 4.0 |
| 64.7 |
| 1(h) + 2 30.0 + 0.25 |
| 16.0 |
| 1(h) + 2 35.0 + 0.50 |
| 44.0 |
| 1(h) + 2 35.0 + 1.0 |
| 31.3 |
| 1(h) + 2 35.0 + 2.0 |
| 58.7 |
| 1(h) + 2 40.0 + 0.25 |
| 48.0 |
| 1(h) + 2 40.0 + 0.50 |
| 32.7 |
| 1(h) + 2 40.0 + 1.0 |
| 42.0 |
| 1(h) + 2 40.0 + 2.0 |
| 68.0 |
| 4 50.0 5.3 |
| 4 100.0 5.3 Increase |
| 4 500.0 48.0 |
| 1(h) + 4 10.0 + 50.0 |
| 35.3 |
| 1(h) + 4 10.0 + 100.0 |
| 27.3 |
| 1(h) + 4 10.0 + 500.0 |
| 47.3 |
| 1(h) + 4 15.0 + 50.0 |
| 12.0 |
| 1(h) + 4 15.0 + 100.0 |
| 4.0 |
| 1(h) + 4 15.0 + 500.0 |
| 17.3 |
| 1(h) + 4 20.0 + 50.0 |
| 29.3 |
| 1(h) + 4 20.0 + 100.0 |
| 34.0 |
| 1(h) + 4 20.0 + 500.0 |
| 50.0 |
| 1(h) + 4 25.0 + 50.0 |
| 54.0 |
| 1(h) + 4 25.0 + 100.0 |
| 63.3 |
| 1(h) + 4 25.0 + 500.0 |
| 12.0 |
| 2 + 4 0.5 + 50.0 |
| 9.3 Increase |
| 2 + 4 0.5 + 100.0 |
| 18.0 Increase |
| 2 + 4 0.5 + 500.0 |
| 36.7 |
| 2 + 4 1.0 + 50.0 |
| 33.3 |
| 2 + 4 1.0 + 100.0 |
| 42.0 |
| 2 + 4 1.0 + 500.0 |
| 48.0 |
| 2 + 4 2.0 + 50.0 |
| 26.7 |
| 2 + 4 2.0 + 100.0 |
| 48.0 |
| 2 + 4 2.0 + 500.0 |
| 75.3 |
| 2 + 4 4.0 + 50.0 |
| 37.3 |
| 2 + 4 4.0 + 100.0 |
| 20.7 |
| 2 + 4 4.0 + 500.0 |
| 33.3 |
| ______________________________________ |
A six foot by twenty foot plot containing a mixed stand of grasses which include tall rescue (Festuca arundinaecae); Kentucky bluegrass (Poa pratensis), annual ryegrass (Lolium mulciforum) and perennial ryegrass (Lolium perenne) is mowed at a height of one and one-half inches. Twenty-four hours after mowing the plot is sprayed with an aqueous solution containing 0.25% by volume of a nonionic surfactant mixture of alkylarylpolyoxyechyleneglycols, free fatty acids, and 2-propanol and formula I (a)-(k) compounds and compounds 2, 3, 4 and 5 alone and in combinations at a variety of concentrations. Sufficient aqueous solution is applied to provide the equivalent of 25 gal/acre of spray. Each treatment is applied co three plots which are situated randomly within the test area and the results for each treatment are obtained by averaging the three replicates. The height of each treatment plot is measured at three weeks and five weeks after treatment to determine the effectiveness of the treatment in retarding growth. Examination of Table VI below which is a summary of the results obtained on the mixed stand of grasses demonstrates the effectiveness of the formula I (a)-(k) compounds alone and additionally demonstrates the improved effectiveness of these formula I (a)-(k) Compounds in combination with compounds 2, 3, 4 and 5 for retarding the growth of turfgrasses.
| TABLE VI |
| ______________________________________ |
| Evaluation of compositions of the invention on a |
| mix stand of grasses which include Tall Fescue |
| (Festuca arundinaecae), Kentucky Bluegrass |
| (Poa pratensis), Annual Ryegrass (Lolium multiforum) |
| and Perennial Ryegrass (Lolium perenne) |
| % Decrease |
| in height |
| Rate(s) 22-25 36-38 |
| Treatments g or lb/A DAT* DAT* |
| ______________________________________ |
| 1(h) 25.0 g 16 -- |
| 1(h) 50.0 g 24 -- |
| 1(h) 75.0 g 10 -- |
| 1(b) 1.0 g 14 -- |
| 1(b) 2.0 g 30 19 |
| 1(b) 2.5 g -- -- |
| 1(b) 5.0 g -- -- |
| 1(d) 25.0 g 10 -- |
| 1(d) 50.0 g 14 -- |
| 1(d) 75.0 g 23 -- |
| 1(a) 20.0 g 38 37 |
| 1(a) 40.0 g 42 40 |
| 1(a) 60.0 g 37 34 |
| 3 5.0 lb 14 -- |
| 5 3.5 g 8 -- |
| 5 7.0 g 4 -- |
| 4 0.5 lb 23 8 |
| 1(h) + 1(b) 25.0 g + 2.5 g |
| -- -- |
| 1(h) + 1(b) 25.0 g + 5.0 g |
| 15 -- |
| 1(h) + 2 25.0 g + 1.0 g |
| 28 -- |
| 1(h) + 2 25.0 g + 2.0 g |
| 29 -- |
| 1(h) + 2 50.0 g + 1.0 g |
| -- 10 |
| 1(h) + 2 50.0 g + 2.0 g |
| 26 12 |
| 1(d) + 2 25.0 g + 1.0 g |
| 23 -- |
| 1(d) + 2 25.0 g + 2.0 g |
| 11 -- |
| 1(h) + 3 25.0 g + 1.5 lb |
| 16 13 |
| 1(h) + 3 50.0 g + 1.5 lb |
| 29 12 |
| 1(h) + 4 25.0 g + 0.125 lb |
| 42 16 |
| 1(h) + 4 50.0 g + 0.125 lb |
| 38 27 |
| 1(h) + 5 20.0 g + 3.5 g |
| 16 -- |
| 1(d) + 4 25.0 g + 0.125 lb |
| 37 13 |
| 1(d) + 5 25.0 g + 3.5 g |
| 19 13 |
| 1(d) + 3 25.0 g + 1.5 lb |
| 31 14 |
| 1(d) + 3 50.0 g + 1.5 lb |
| 29 14 |
| 1(k) 20.0 g 27 -- |
| 1(k) 40.0 g 29 11 |
| 1(k) 60.0 g 24 31 |
| 1(k) 80.0 g 37 41 |
| 1(d) 20.0 g 22 -- |
| 1(d) 40.0 g 24 -- |
| 1(d) 60.0 g 19 -- |
| 1(d) 80.0 g 35 23 |
| 2 1.0 g -- -- |
| 2 2.0 g -- 7.2 |
| 1(k) + 2 20.0 g + 1.0 g |
| 21 16 |
| 1(k) + 2 20.0 g + 2.0 g |
| 28 25 |
| 1(k) + 2 40.0 g + 1.0 g |
| 22 34 |
| 1(k) + 2 40.0 g + 2.0 g |
| 32 30 |
| 1(d) + 2 20.0 g + 1.0 g |
| 16 -- |
| 1(d) + 2 20.0 g + 2.0 g |
| 19 13 |
| 1(d) + 2 40.0 g + 1.0 g |
| 19 -- |
| 1(d) + 2 40.0 g + 2.0 g |
| 26 29 |
| 4 0.125 lb 26 29 |
| 4 0.375 lb 15 19 |
| 4 + 2 0.125 lb + 1 g |
| 34 29 |
| 4 + 2 0.125 lb + 2 g |
| 38 25 |
| 4 + 1(k) 0.125 lb + 20 g |
| 31 23 |
| 4 + 1(d) 0.125 lb + 20 g |
| 29 13.5 |
| 5 2.0 g -- -- |
| 5 7.0 g 15 -- |
| 5 + 2 2.0 g + 1.0 g |
| 21 4 |
| 5 + 4 + 2 2.0 g + 0.125 g + |
| 28 5.8 |
| 1.0 g |
| 5 + 4 + 1(d) |
| 2.0 g + 0.125 g + |
| 27 -- |
| 20.0 g |
| 5 + 4 + 1(k) |
| 2.0 g + 0.125 g + |
| 44 10 |
| 20.0 g |
| ______________________________________ |
| *DAT = Days after treatment |
An evaluation of another composition of the invention is conducted using the procedure of Example 1 above and Bermudagrass (Cynodon doctylon) as the turfgrass species.
The test composition, 2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-yl)-5-methyl-nicotinic acid, is applied to said turfgrass at rates of from 25 to 200 grams per hectare. Test compound is applied in the form of an aqueous solution as described in Example 1 and treated plants were held in the greenhouse for 60 days after treatment and then harvested.
Data obtained are reported in Table VII below.
| TABLE VII |
| ______________________________________ |
| Rate Phytotoxicity |
| Clipping* Clipping* |
| (g/ha) |
| Rating** Fresh Weight (g) |
| Dry Weight (g) |
| ______________________________________ |
| 0 0 369 97 |
| 25 0 231 (37.4%) 59 (39.1%) |
| 50 0 209 (43.3%) 54 (44.3%) |
| 100 1 163 (55.8%) 41 (57.7%) |
| 150 3 114 (69.1%) 30 (69.0%) |
| 200 5 68 (81.5%) 23 (76.2%) |
| ______________________________________ |
| *% Reduction over checks is shown in parenthesis. |
| **Phytotoxicity Rating ranges from 0 meaning no injury to 10 meaning |
| complete kill. |
Bhalla, Prithvi Raj, Herrick, Robert Michael, Gates, Donald Wakeford
| Patent | Priority | Assignee | Title |
| Patent | Priority | Assignee | Title |
| 4608079, | Aug 02 1983 | American Cyanamid Company | Imidazolidinones, and imidazolidinethiones, process and intermediates for the preparation thereof, and use of said compounds as herbicidal agents |
| 4957536, | Jun 02 1980 | American Cyanamid Company | Method for increasing axillary branching, tillering, flowering and yield of agronomic and horticultural crops with certain 2-(2-imidazolin-2-yl)-pyridines and quinolines |
| Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
| May 26 1995 | American Cyanamid Company | (assignment on the face of the patent) | / |
| Date | Maintenance Fee Events |
| Date | Maintenance Schedule |
| Jan 06 2001 | 4 years fee payment window open |
| Jul 06 2001 | 6 months grace period start (w surcharge) |
| Jan 06 2002 | patent expiry (for year 4) |
| Jan 06 2004 | 2 years to revive unintentionally abandoned end. (for year 4) |
| Jan 06 2005 | 8 years fee payment window open |
| Jul 06 2005 | 6 months grace period start (w surcharge) |
| Jan 06 2006 | patent expiry (for year 8) |
| Jan 06 2008 | 2 years to revive unintentionally abandoned end. (for year 8) |
| Jan 06 2009 | 12 years fee payment window open |
| Jul 06 2009 | 6 months grace period start (w surcharge) |
| Jan 06 2010 | patent expiry (for year 12) |
| Jan 06 2012 | 2 years to revive unintentionally abandoned end. (for year 12) |